Cleaning Validation Plates & Cleaning Validation Coupons Supplier for Pharmaceutical Labs in India

SS304 – Full Cleaning Validation Description SS304 Cleaning Validation Coupons are designed to represent SS304 Cleaning Validation Coupons replicate the most widely used stainless steel surface in pharmaceutical equipment. They represent 18-8 chromium-nickel steel surfaces found in tanks, pipelines and contact parts. SS304 offers good corrosion resistance and stable residue recovery under GMP conditions. Used for swab recovery, rinse recovery and detergent effectiveness studies. Ideal for validating cleaning procedures on standard stainless-steel contact equipment.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from SS304. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for SS304 surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from SS304 ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: SS304 Cleaning Validation Coupons replicate the most widely used stainless steel surface in pharmaceutical equipment. They represent 18-8 chromium-nickel steel surfaces found in tanks, pipelines and contact parts. SS304 offers good corrosion resistance and stable residue recovery under GMP conditions. Used for swab recovery, rinse recovery and detergent effectiveness studies. Ideal for validating cleaning procedures on standard stainless-steel contact equipment. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

ABS – Full Cleaning Validation Description ABS Cleaning Validation Coupons are designed to represent ABS Cleaning Validation Coupons simulate polymer equipment surfaces commonly found in housings and plastic components. They help evaluate cleanability and residue recovery from non-metallic contact surfaces. ABS is impact-resistant with moderate chemical compatibility and stable surface recovery behavior. Supports GMP-compliant swab and rinse recovery for polymer-based equipment. Ideal for validating cleaning procedures involving plastic or molded parts.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from ABS. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for ABS surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from ABS ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: ABS Cleaning Validation Coupons simulate polymer equipment surfaces commonly found in housings and plastic components. They help evaluate cleanability and residue recovery from non-metallic contact surfaces. ABS is impact-resistant with moderate chemical compatibility and stable surface recovery behavior. Supports GMP-compliant swab and rinse recovery for polymer-based equipment. Ideal for validating cleaning procedures involving plastic or molded parts. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

SS316L – Full Cleaning Validation Description SS316L Cleaning Validation Coupons are designed to represent SS316L Cleaning Validation Coupons replicate high-purity stainless-steel surfaces used in aggressive processing zones. The molybdenum-enriched alloy provides superior resistance to chlorides and acidic detergents. Used for validating cleanability in CIP/SIP systems, tanks, reactors and high-sanitization equipment. Delivers consistent swab recovery and surface reproducibility under GMP. Essential for verifying cleaning procedures on 316L contact surfaces.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from SS316L. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for SS316L surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from SS316L ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: SS316L Cleaning Validation Coupons replicate high-purity stainless-steel surfaces used in aggressive processing zones. The molybdenum-enriched alloy provides superior resistance to chlorides and acidic detergents. Used for validating cleanability in CIP/SIP systems, tanks, reactors and high-sanitization equipment. Delivers consistent swab recovery and surface reproducibility under GMP. Essential for verifying cleaning procedures on 316L contact surfaces. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Acrylic/Plexiglass – Full Cleaning Validation Description Acrylic/Plexiglass Cleaning Validation Coupons are designed to represent Acrylic/Plexiglass Cleaning Validation Coupons simulate transparent polymeric surfaces used in covers and viewing windows. They represent smooth, non-metallic surfaces with controlled residue recovery behavior. Useful for evaluating cleaning effectiveness on polymer sheets used in containment areas. Chemically stable against mild detergents and alcohol-based cleaners. Ideal for validating cleaning procedures on acrylic enclosures and housings.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Acrylic/Plexiglass. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Acrylic/Plexiglass surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Acrylic/Plexiglass ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Acrylic/Plexiglass Cleaning Validation Coupons simulate transparent polymeric surfaces used in covers and viewing windows. They represent smooth, non-metallic surfaces with controlled residue recovery behavior. Useful for evaluating cleaning effectiveness on polymer sheets used in containment areas. Chemically stable against mild detergents and alcohol-based cleaners. Ideal for validating cleaning procedures on acrylic enclosures and housings. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Aluminium – Full Cleaning Validation Description Aluminium Cleaning Validation Coupons are designed to represent Aluminium Cleaning Validation Coupons represent lightweight non-ferrous surfaces used in pharma equipment. They simulate machined aluminium housings, guards, frames, and structural components. Aluminium offers good corrosion resistance and predictable residue recovery behaviour. Useful for swab and rinse recovery studies involving aluminium materials of construction. Ideal for validating cleaning procedures on aluminium surfaces under GMP requirements.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Aluminium. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Aluminium surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Aluminium ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Aluminium Cleaning Validation Coupons represent lightweight non-ferrous surfaces used in pharma equipment. They simulate machined aluminium housings, guards, frames, and structural components. Aluminium offers good corrosion resistance and predictable residue recovery behaviour. Useful for swab and rinse recovery studies involving aluminium materials of construction. Ideal for validating cleaning procedures on aluminium surfaces under GMP requirements. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Ceramic – Full Cleaning Validation Description Ceramic Cleaning Validation Coupons are designed to represent Ceramic Cleaning Validation Coupons replicate hard, chemically resistant ceramic surfaces used in pharma processing. They provide stable, non-porous surfaces for consistent residue recovery. Ideal for validating equipment zones containing ceramic insulators, seals or liners. Ceramics resist high temperatures, harsh cleaners and repeated cleaning cycles. Useful for worst-case cleanability studies on non-metallic inorganic surfaces.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Ceramic. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Ceramic surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Ceramic ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Ceramic Cleaning Validation Coupons replicate hard, chemically resistant ceramic surfaces used in pharma processing. They provide stable, non-porous surfaces for consistent residue recovery. Ideal for validating equipment zones containing ceramic insulators, seals or liners. Ceramics resist high temperatures, harsh cleaners and repeated cleaning cycles. Useful for worst-case cleanability studies on non-metallic inorganic surfaces. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Cast – Full Cleaning Validation Description Cast Cleaning Validation Coupons are designed to represent Cast Iron Cleaning Validation Coupons simulate iron-carbon alloy surfaces used in heavy-duty pharma equipment components. They represent robust mechanical parts with specific residue retention behavior. Useful for swab and rinse recovery studies where cast iron is part of the assembly. Supports validation of cleaning effectiveness on ferrous alloy surfaces. Ideal for covering all MoCs in mixed-metal systems.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Cast. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Cast surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Cast ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Cast Iron Cleaning Validation Coupons simulate iron-carbon alloy surfaces used in heavy-duty pharma equipment components. They represent robust mechanical parts with specific residue retention behavior. Useful for swab and rinse recovery studies where cast iron is part of the assembly. Supports validation of cleaning effectiveness on ferrous alloy surfaces. Ideal for covering all MoCs in mixed-metal systems. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Aluminium – Full Cleaning Validation Description Aluminium Cleaning Validation Coupons are designed to represent Aluminium Cleaning Validation Coupons represent lightweight non-ferrous surfaces used in pharma equipment. They simulate machined aluminium housings, guards, frames, and structural components. Aluminium offers good corrosion resistance and predictable residue recovery behaviour. Useful for swab and rinse recovery studies involving aluminium materials of construction. Ideal for validating cleaning procedures on aluminium surfaces under GMP requirements.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Aluminium. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Aluminium surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Aluminium ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Aluminium Cleaning Validation Coupons represent lightweight non-ferrous surfaces used in pharma equipment. They simulate machined aluminium housings, guards, frames, and structural components. Aluminium offers good corrosion resistance and predictable residue recovery behaviour. Useful for swab and rinse recovery studies involving aluminium materials of construction. Ideal for validating cleaning procedures on aluminium surfaces under GMP requirements. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Anodized – Full Cleaning Validation Description Anodized Cleaning Validation Coupons are designed to represent Anodized Aluminium 6061 Cleaning Validation Coupons represent hardened oxide-coated aluminium surfaces. They simulate anodized equipment components such as housings, guards, brackets and instrument frames. Anodizing enhances corrosion resistance, hardness and surface stability during cleaning. Useful for swab and rinse recovery studies involving anodized aluminium construction. Ideal for validating GMP cleaning procedures on protective oxide-coated aluminium surfaces.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Anodized. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Anodized surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Anodized ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Anodized Aluminium 6061 Cleaning Validation Coupons represent hardened oxide-coated aluminium surfaces. They simulate anodized equipment components such as housings, guards, brackets and instrument frames. Anodizing enhances corrosion resistance, hardness and surface stability during cleaning. Useful for swab and rinse recovery studies involving anodized aluminium construction. Ideal for validating GMP cleaning procedures on protective oxide-coated aluminium surfaces. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Bronze – Full Cleaning Validation Description Bronze Cleaning Validation Coupons are designed to represent Bronze Cleaning Validation Coupons represent copper–tin alloy surfaces used in pharmaceutical equipment parts. They simulate bronze bushings, bearings, pump sections and wear-resistant areas. Bronze provides good strength, corrosion resistance and predictable residue recovery. Useful for swab and rinse validation of bronze-contact zones. Ideal for validating cleaning procedures involving bronze components under GMP guidelines.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Bronze. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Bronze surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Bronze ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Bronze Cleaning Validation Coupons represent copper–tin alloy surfaces used in pharmaceutical equipment parts. They simulate bronze bushings, bearings, pump sections and wear-resistant areas. Bronze provides good strength, corrosion resistance and predictable residue recovery. Useful for swab and rinse validation of bronze-contact zones. Ideal for validating cleaning procedures involving bronze components under GMP guidelines. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Brass – Full Cleaning Validation Description Brass Cleaning Validation Coupons are designed to represent Brass 353 Cleaning Validation Coupons represent high-leaded free-machining brass surfaces. They simulate precision-turned parts, valves, fittings and threaded components. Brass 353 offers excellent machinability and stable residue recovery characteristics. Useful for validating cleaning of high-lead brass contact parts under GMP. Ideal for swab and rinse recovery studies on free-machining brass components.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Brass. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Brass surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Brass ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Brass 353 Cleaning Validation Coupons represent high-leaded free-machining brass surfaces. They simulate precision-turned parts, valves, fittings and threaded components. Brass 353 offers excellent machinability and stable residue recovery characteristics. Useful for validating cleaning of high-lead brass contact parts under GMP. Ideal for swab and rinse recovery studies on free-machining brass components. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Brass – Full Cleaning Validation Description Brass Cleaning Validation Coupons are designed to represent Brass 353 Cleaning Validation Coupons represent high-leaded free-machining brass surfaces. They simulate precision-turned parts, valves, fittings and threaded components. Brass 353 offers excellent machinability and stable residue recovery characteristics. Useful for validating cleaning of high-lead brass contact parts under GMP. Ideal for swab and rinse recovery studies on free-machining brass components.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Brass. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Brass surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Brass ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Brass 353 Cleaning Validation Coupons represent high-leaded free-machining brass surfaces. They simulate precision-turned parts, valves, fittings and threaded components. Brass 353 offers excellent machinability and stable residue recovery characteristics. Useful for validating cleaning of high-lead brass contact parts under GMP. Ideal for swab and rinse recovery studies on free-machining brass components. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

EPDM – Full Cleaning Validation Description EPDM Cleaning Validation Coupons are designed to represent EPDM Cleaning Validation Coupons simulate ethylene–propylene–diene rubber surfaces used in seals and gaskets. They represent flexible elastomer contact parts. EPDM offers excellent chemical and heat resistance. Useful for swab/rinse recovery on elastomer zones. Ideal for GMP cleaning validation involving rubber components.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from EPDM. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for EPDM surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from EPDM ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: EPDM Cleaning Validation Coupons simulate ethylene–propylene–diene rubber surfaces used in seals and gaskets. They represent flexible elastomer contact parts. EPDM offers excellent chemical and heat resistance. Useful for swab/rinse recovery on elastomer zones. Ideal for GMP cleaning validation involving rubber components. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Epoxy – Full Cleaning Validation Description Epoxy Cleaning Validation Coupons are designed to represent Epoxy Reinforced Resin Cleaning Validation Coupons simulate thermoset resin components used in pharma systems. They represent reinforced composite surfaces found in housings, panels and equipment covers. Epoxy resin offers excellent chemical resistance and dimensional stability. Useful for swab/rinse recovery on composite materials. Ideal for GMP cleaning validation of reinforced resin parts.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Epoxy. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Epoxy surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Epoxy ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Epoxy Reinforced Resin Cleaning Validation Coupons simulate thermoset resin components used in pharma systems. They represent reinforced composite surfaces found in housings, panels and equipment covers. Epoxy resin offers excellent chemical resistance and dimensional stability. Useful for swab/rinse recovery on composite materials. Ideal for GMP cleaning validation of reinforced resin parts. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

FEP – Full Cleaning Validation Description FEP Cleaning Validation Coupons are designed to represent FEP Cleaning Validation Coupons simulate fluorinated ethylene propylene surfaces used in high‑purity pharmaceutical tubing, liners and non‑stick polymer components. FEP is chemically inert, solvent‑resistant and ultra‑low adhesion. Ideal for worst‑case swab and rinse recovery studies. Supports GMP validation for fluoropolymer equipment.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from FEP. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for FEP surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from FEP ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: FEP Cleaning Validation Coupons simulate fluorinated ethylene propylene surfaces used in high‑purity pharmaceutical tubing, liners and non‑stick polymer components. FEP is chemically inert, solvent‑resistant and ultra‑low adhesion. Ideal for worst‑case swab and rinse recovery studies. Supports GMP validation for fluoropolymer equipment. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Borosilicate – Full Cleaning Validation Description Borosilicate Cleaning Validation Coupons are designed to represent Borosilicate Glass Cleaning Validation Coupons simulate high‑purity glass contact surfaces used in pharmaceutical vessels, vials and analytical equipment. They offer excellent chemical resistance and thermal stability. Ideal for swab and rinse recovery studies on glass MoCs. Supports GMP cleaning validation for glassware‑based systems.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Borosilicate. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Borosilicate surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Borosilicate ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Borosilicate Glass Cleaning Validation Coupons simulate high‑purity glass contact surfaces used in pharmaceutical vessels, vials and analytical equipment. They offer excellent chemical resistance and thermal stability. Ideal for swab and rinse recovery studies on glass MoCs. Supports GMP cleaning validation for glassware‑based systems. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Toughened – Full Cleaning Validation Description Toughened Cleaning Validation Coupons are designed to represent Toughened Glass Cleaning Validation Coupons simulate chemically strengthened glass surfaces used in pharma equipment windows, protective shields and viewing panels. Highly durable, impact-resistant and thermally stable. Ideal for swab/rinse recovery studies on strengthened glass.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Toughened. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Toughened surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Toughened ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Toughened Glass Cleaning Validation Coupons simulate chemically strengthened glass surfaces used in pharma equipment windows, protective shields and viewing panels. Highly durable, impact-resistant and thermally stable. Ideal for swab/rinse recovery studies on strengthened glass. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Hastelloy – Full Cleaning Validation Description Hastelloy Cleaning Validation Coupons are designed to represent Hastelloy C-276 Cleaning Validation Coupons simulate nickel–molybdenum–chromium alloy surfaces used in highly corrosive pharmaceutical and bioprocess environments. C‑276 provides exceptional resistance to chlorides, acids and oxidizers. Ideal for worst‑case cleaning validation in harsh CIP/SIP chemistry. Supports RF% studies on high‑alloy corrosion‑resistant MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Hastelloy. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Hastelloy surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Hastelloy ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Hastelloy C-276 Cleaning Validation Coupons simulate nickel–molybdenum–chromium alloy surfaces used in highly corrosive pharmaceutical and bioprocess environments. C‑276 provides exceptional resistance to chlorides, acids and oxidizers. Ideal for worst‑case cleaning validation in harsh CIP/SIP chemistry. Supports RF% studies on high‑alloy corrosion‑resistant MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Hastelloy – Full Cleaning Validation Description Hastelloy Cleaning Validation Coupons are designed to represent Hastelloy C-276 Cleaning Validation Coupons simulate nickel–molybdenum–chromium alloy surfaces used in highly corrosive pharmaceutical and bioprocess environments. C‑276 provides exceptional resistance to chlorides, acids and oxidizers. Ideal for worst‑case cleaning validation in harsh CIP/SIP chemistry. Supports RF% studies on high‑alloy corrosion‑resistant MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Hastelloy. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Hastelloy surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Hastelloy ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Hastelloy C-276 Cleaning Validation Coupons simulate nickel–molybdenum–chromium alloy surfaces used in highly corrosive pharmaceutical and bioprocess environments. C‑276 provides exceptional resistance to chlorides, acids and oxidizers. Ideal for worst‑case cleaning validation in harsh CIP/SIP chemistry. Supports RF% studies on high‑alloy corrosion‑resistant MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

HCHC – Full Cleaning Validation Description HCHC Cleaning Validation Coupons are designed to represent HCHC high-carbon, high-chromium alloy coupons simulate hardened tool steel surfaces used in pharma cutting, granulation and contact tooling. Extremely wear-resistant and moderately corrosion‑resistant. Ideal for swab recovery and validating cleaning of high-hardness steel surfaces.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from HCHC. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for HCHC surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from HCHC ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: HCHC high-carbon, high-chromium alloy coupons simulate hardened tool steel surfaces used in pharma cutting, granulation and contact tooling. Extremely wear-resistant and moderately corrosion‑resistant. Ideal for swab recovery and validating cleaning of high-hardness steel surfaces. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

HDPE – Full Cleaning Validation Description HDPE Cleaning Validation Coupons are designed to represent HDPE (High Density Polyethylene) Cleaning Validation Coupons simulate polyolefin contact surfaces used in pharma containers, liners and transfer components. HDPE offers excellent chemical resistance, low extractables and good cleanability. Ideal for swab/rinse recovery on plastic MoCs. Supports GMP validation of polyethylene-based equipment parts.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from HDPE. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for HDPE surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from HDPE ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: HDPE (High Density Polyethylene) Cleaning Validation Coupons simulate polyolefin contact surfaces used in pharma containers, liners and transfer components. HDPE offers excellent chemical resistance, low extractables and good cleanability. Ideal for swab/rinse recovery on plastic MoCs. Supports GMP validation of polyethylene-based equipment parts. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Hypalon – Full Cleaning Validation Description Hypalon Cleaning Validation Coupons are designed to represent Hypalon (CSM Rubber) Cleaning Validation Coupons simulate chlorosulfonated polyethylene surfaces used in chemical-resistant pharma seals and linings. Excellent resistance to acids, oxidizers and weathering. Ideal for validating cleaning on durable elastomer surfaces.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Hypalon. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Hypalon surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Hypalon ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Hypalon (CSM Rubber) Cleaning Validation Coupons simulate chlorosulfonated polyethylene surfaces used in chemical-resistant pharma seals and linings. Excellent resistance to acids, oxidizers and weathering. Ideal for validating cleaning on durable elastomer surfaces. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

LDPE – Full Cleaning Validation Description LDPE Cleaning Validation Coupons are designed to represent LDPE (Low Density Polyethylene) Cleaning Validation Coupons model flexible polyolefin surfaces used in liners, bags and pharma packaging. LDPE provides good chemical resistance, low extractables and moderate cleanability. Ideal for GMP swab and rinse recovery studies on soft plastic MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from LDPE. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for LDPE surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from LDPE ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: LDPE (Low Density Polyethylene) Cleaning Validation Coupons model flexible polyolefin surfaces used in liners, bags and pharma packaging. LDPE provides good chemical resistance, low extractables and moderate cleanability. Ideal for GMP swab and rinse recovery studies on soft plastic MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

NBR – Full Cleaning Validation Description NBR Cleaning Validation Coupons are designed to represent NBR (Nitrile Butadiene Rubber, Buna‑N) Cleaning Validation Coupons simulate oil‑resistant elastomer surfaces used in gaskets, hoses and seals. NBR offers excellent resistance to oils, solvents and fuels. Ideal for validating cleaning of chemically exposed rubber MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from NBR. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for NBR surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from NBR ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: NBR (Nitrile Butadiene Rubber, Buna‑N) Cleaning Validation Coupons simulate oil‑resistant elastomer surfaces used in gaskets, hoses and seals. NBR offers excellent resistance to oils, solvents and fuels. Ideal for validating cleaning of chemically exposed rubber MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Neoprene – Full Cleaning Validation Description Neoprene Cleaning Validation Coupons are designed to represent Neoprene Rubber (Polychloroprene) Cleaning Validation Coupons simulate durable elastomer surfaces used in gaskets, hoses and vibration‑resistant seals. Neoprene offers strong resistance to oils, oxidation and moderate chemicals, making it ideal for validating cleaning of flexible rubber MoCs in GMP environments.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Neoprene. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Neoprene surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Neoprene ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Neoprene Rubber (Polychloroprene) Cleaning Validation Coupons simulate durable elastomer surfaces used in gaskets, hoses and vibration‑resistant seals. Neoprene offers strong resistance to oils, oxidation and moderate chemicals, making it ideal for validating cleaning of flexible rubber MoCs in GMP environments. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Nylon – Full Cleaning Validation Description Nylon Cleaning Validation Coupons are designed to represent Nylon 6/12 Cleaning Validation Coupons represent low-moisture-absorption polyamide surfaces used in engineering components, fittings and wear-resistant parts. Offers excellent dimensional stability and moderate chemical resistance. Ideal for validating cleaning on rigid polymer MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Nylon. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Nylon surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Nylon ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Nylon 6/12 Cleaning Validation Coupons represent low-moisture-absorption polyamide surfaces used in engineering components, fittings and wear-resistant parts. Offers excellent dimensional stability and moderate chemical resistance. Ideal for validating cleaning on rigid polymer MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Non-Woven – Full Cleaning Validation Description Non-Woven Cleaning Validation Coupons are designed to represent Non-Woven Fiber Cleaning Validation Coupons replicate fibrous polymer surfaces used in filters, wipes, liners, soft components and porous media. They allow validation of cleaning and residue removal on absorbent, textured surfaces commonly present in GMP operations.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Non-Woven. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Non-Woven surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Non-Woven ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Non-Woven Fiber Cleaning Validation Coupons replicate fibrous polymer surfaces used in filters, wipes, liners, soft components and porous media. They allow validation of cleaning and residue removal on absorbent, textured surfaces commonly present in GMP operations. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

PEEK – Full Cleaning Validation Description PEEK Cleaning Validation Coupons are designed to represent PEEK Cleaning Validation Coupons simulate high-performance engineering polymer surfaces used in critical GMP equipment. They provide excellent chemical resistance, thermal stability and represent polymeric contact parts requiring validated cleaning performance.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from PEEK. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for PEEK surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from PEEK ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: PEEK Cleaning Validation Coupons simulate high-performance engineering polymer surfaces used in critical GMP equipment. They provide excellent chemical resistance, thermal stability and represent polymeric contact parts requiring validated cleaning performance. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Polycarbonate – Full Cleaning Validation Description Polycarbonate Cleaning Validation Coupons are designed to represent Polycarbonate Cleaning Validation Coupons represent transparent, high-impact plastic surfaces used in equipment guards, windows and covers. They provide moderate chemical resistance and good durability, making them essential surfaces for residue recovery assessment.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Polycarbonate. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Polycarbonate surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Polycarbonate ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Polycarbonate Cleaning Validation Coupons represent transparent, high-impact plastic surfaces used in equipment guards, windows and covers. They provide moderate chemical resistance and good durability, making them essential surfaces for residue recovery assessment. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

PET-G – Full Cleaning Validation Description PET-G Cleaning Validation Coupons are designed to represent PET-G Cleaning Validation Coupons represent glycol-modified polyethylene terephthalate surfaces. They offer excellent clarity, impact resistance and moderate chemical stability—important for validating cleaning on polymer housings, covers and transparent equipment components in GMP facilities.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from PET-G. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for PET-G surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from PET-G ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: PET-G Cleaning Validation Coupons represent glycol-modified polyethylene terephthalate surfaces. They offer excellent clarity, impact resistance and moderate chemical stability—important for validating cleaning on polymer housings, covers and transparent equipment components in GMP facilities. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

PET-P – Full Cleaning Validation Description PET-P Cleaning Validation Coupons are designed to represent PET-P Cleaning Validation Coupons represent high-crystallinity polyester surfaces with strong chemical resistance and excellent dimensional stability. Ideal for validating cleaning procedures on rigid polymer components in GMP processing environments.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from PET-P. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for PET-P surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from PET-P ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: PET-P Cleaning Validation Coupons represent high-crystallinity polyester surfaces with strong chemical resistance and excellent dimensional stability. Ideal for validating cleaning procedures on rigid polymer components in GMP processing environments. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

POM‑C – Full Cleaning Validation Description POM‑C Cleaning Validation Coupons are designed to represent POM‑C Cleaning Validation Coupons represent acetal engineering plastic surfaces with high stiffness, excellent dimensional stability, and strong chemical resistance. They support validating residue removal from precision polymer components in GMP environments.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from POM‑C. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for POM‑C surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from POM‑C ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: POM‑C Cleaning Validation Coupons represent acetal engineering plastic surfaces with high stiffness, excellent dimensional stability, and strong chemical resistance. They support validating residue removal from precision polymer components in GMP environments. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

PVDC – Full Cleaning Validation Description PVDC Cleaning Validation Coupons are designed to represent PVDC Cleaning Validation Coupons represent high-barrier polymer surfaces used in pharmaceutical packaging contact, blister materials, and barrier films. PVDC offers exceptional chemical resistance and low permeability, making it a valuable material for evaluating cleaning under GMP conditions.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from PVDC. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for PVDC surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from PVDC ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: PVDC Cleaning Validation Coupons represent high-barrier polymer surfaces used in pharmaceutical packaging contact, blister materials, and barrier films. PVDC offers exceptional chemical resistance and low permeability, making it a valuable material for evaluating cleaning under GMP conditions. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Polyester – Full Cleaning Validation Description Polyester Cleaning Validation Coupons are designed to represent Polyester Cleaning Validation Coupons represent durable polymer surfaces with good chemical stability, high mechanical strength, and low moisture absorption, making them suitable for validating cleaning procedures on polymeric equipment components under GMP conditions.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Polyester. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Polyester surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Polyester ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Polyester Cleaning Validation Coupons represent durable polymer surfaces with good chemical stability, high mechanical strength, and low moisture absorption, making them suitable for validating cleaning procedures on polymeric equipment components under GMP conditions. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Polyamide – Full Cleaning Validation Description Polyamide Cleaning Validation Coupons are designed to represent Polyamide Cleaning Validation Coupons simulate strong engineering polymer surfaces. They provide GMP-compliant residue recovery verification for polymer components exposed to detergents, disinfectants, and mechanical stress in pharmaceutical equipment.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Polyamide. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Polyamide surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Polyamide ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Polyamide Cleaning Validation Coupons simulate strong engineering polymer surfaces. They provide GMP-compliant residue recovery verification for polymer components exposed to detergents, disinfectants, and mechanical stress in pharmaceutical equipment. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Polyurethane – Full Cleaning Validation Description Polyurethane Cleaning Validation Coupons are designed to represent Polyurethane Cleaning Validation Coupons represent flexible, abrasion‑resistant polymer surfaces used in GMP systems. They verify cleaning effectiveness on elastomeric parts exposed to detergents and mechanical stress. Polyurethane’s resilience ensures reliable swab and rinse recovery accuracy. These coupons support validation of seals, rollers, wipers, and tubing components. Ideal for demonstrating regulatory compliance for dynamic polymer MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Polyurethane. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Polyurethane surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Polyurethane ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Polyurethane Cleaning Validation Coupons represent flexible, abrasion‑resistant polymer surfaces used in GMP systems. They verify cleaning effectiveness on elastomeric parts exposed to detergents and mechanical stress. Polyurethane’s resilience ensures reliable swab and rinse recovery accuracy. These coupons support validation of seals, rollers, wipers, and tubing components. Ideal for demonstrating regulatory compliance for dynamic polymer MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

PVC – Full Cleaning Validation Description PVC Cleaning Validation Coupons are designed to represent PVC Cleaning Validation Coupons represent rigid polyvinyl chloride equipment surfaces used in GMP utilities. They simulate plastic piping, housings, and protective covers that contact cleaning agents. PVC coupons support residue recovery studies for non‑metallic utility components. Their chemical stability helps evaluate detergent and disinfectant compatibility. They enable RF% determination for polymer MoCs in validated cleaning procedures. Ideal for documenting regulatory compliance for PVC-based process and utility hardware.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from PVC. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for PVC surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from PVC ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: PVC Cleaning Validation Coupons represent rigid polyvinyl chloride equipment surfaces used in GMP utilities. They simulate plastic piping, housings, and protective covers that contact cleaning agents. PVC coupons support residue recovery studies for non‑metallic utility components. Their chemical stability helps evaluate detergent and disinfectant compatibility. They enable RF% determination for polymer MoCs in validated cleaning procedures. Ideal for documenting regulatory compliance for PVC-based process and utility hardware. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

POM‑H – Full Cleaning Validation Description POM‑H Cleaning Validation Coupons are designed to represent POM‑H Cleaning Validation Coupons represent high‑strength polyoxymethylene homopolymer surfaces used in GMP systems. They simulate precision plastic components such as gears, valves, housings and guides. POM‑H offers high stiffness, wear‑resistance and low moisture absorption, enabling accurate RF% studies. These coupons help evaluate detergent compatibility for rigid engineering plastics. POM‑H provides excellent dimensional stability for reproducible cleaning validation. Ideal for validating cleaning on high‑precision polymer equipment parts.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from POM‑H. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for POM‑H surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from POM‑H ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: POM‑H Cleaning Validation Coupons represent high‑strength polyoxymethylene homopolymer surfaces used in GMP systems. They simulate precision plastic components such as gears, valves, housings and guides. POM‑H offers high stiffness, wear‑resistance and low moisture absorption, enabling accurate RF% studies. These coupons help evaluate detergent compatibility for rigid engineering plastics. POM‑H provides excellent dimensional stability for reproducible cleaning validation. Ideal for validating cleaning on high‑precision polymer equipment parts. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Polyacetal – Full Cleaning Validation Description Polyacetal Cleaning Validation Coupons are designed to represent Polyacetal Resin (POM) Cleaning Validation Coupons represent rigid engineering‑grade acetal surfaces commonly used in pharmaceutical equipment. They simulate precision components such as gears, rollers, housings, and valve blocks. Their low moisture absorption ensures dimensional stability during RF% studies. POM offers excellent wear resistance, supporting accurate cleaning validation. Ideal for evaluating residue recovery on high‑strength polymer MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Polyacetal. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Polyacetal surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Polyacetal ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Polyacetal Resin (POM) Cleaning Validation Coupons represent rigid engineering‑grade acetal surfaces commonly used in pharmaceutical equipment. They simulate precision components such as gears, rollers, housings, and valve blocks. Their low moisture absorption ensures dimensional stability during RF% studies. POM offers excellent wear resistance, supporting accurate cleaning validation. Ideal for evaluating residue recovery on high‑strength polymer MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Polypropylene – Full Cleaning Validation Description Polypropylene Cleaning Validation Coupons are designed to represent Polypropylene (PP) Cleaning Validation Coupons represent chemically resistant polymer surfaces used in GMP utilities. They simulate containers, piping, housings, and liners widely used in pharma operations. PP offers excellent resistance to detergents, acids, and disinfectants, enabling reliable RF% studies. These coupons help assess cleaning performance on non-metallic contact surfaces. PP provides stable, low-absorption behavior for consistent residue recovery. Ideal for validating cleaning on rigid or translucent polypropylene components.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Polypropylene. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Polypropylene surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Polypropylene ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Polypropylene (PP) Cleaning Validation Coupons represent chemically resistant polymer surfaces used in GMP utilities. They simulate containers, piping, housings, and liners widely used in pharma operations. PP offers excellent resistance to detergents, acids, and disinfectants, enabling reliable RF% studies. These coupons help assess cleaning performance on non-metallic contact surfaces. PP provides stable, low-absorption behavior for consistent residue recovery. Ideal for validating cleaning on rigid or translucent polypropylene components. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

PTFE – Full Cleaning Validation Description PTFE Cleaning Validation Coupons are designed to represent PTFE Cleaning Validation Coupons simulate ultra‑nonstick fluoropolymer surfaces used in GMP systems. They represent Teflon contact parts such as gaskets, seals, tubing, and lining materials. PTFE is chemically inert and resists nearly all detergents and disinfectants, enabling accurate RF% studies. Its low surface energy makes residue recovery validation essential. PTFE’s temperature and chemical stability support robust cleaning validation. Ideal for validating cleaning of fluoropolymer‑lined equipment.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from PTFE. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for PTFE surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from PTFE ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: PTFE Cleaning Validation Coupons simulate ultra‑nonstick fluoropolymer surfaces used in GMP systems. They represent Teflon contact parts such as gaskets, seals, tubing, and lining materials. PTFE is chemically inert and resists nearly all detergents and disinfectants, enabling accurate RF% studies. Its low surface energy makes residue recovery validation essential. PTFE’s temperature and chemical stability support robust cleaning validation. Ideal for validating cleaning of fluoropolymer‑lined equipment. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Silicone – Full Cleaning Validation Description Silicone Cleaning Validation Coupons are designed to represent Silicone USP Grade VI Cleaning Validation Coupons simulate medical‑grade elastomer surfaces. They represent seals, gaskets, diaphragms and flexible interfaces used in sterile pharma systems. Silicone is biocompatible, chemically stable and thermally resistant, supporting accurate RF% studies. Its elastic surface requires validation of residue removal after compression and flex cycles. Ideal for CIP/SIP‑exposed elastomeric contact parts. Ensures compliance for polymer MoCs used in sterile and critical applications.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Silicone. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Silicone surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Silicone ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Silicone USP Grade VI Cleaning Validation Coupons simulate medical‑grade elastomer surfaces. They represent seals, gaskets, diaphragms and flexible interfaces used in sterile pharma systems. Silicone is biocompatible, chemically stable and thermally resistant, supporting accurate RF% studies. Its elastic surface requires validation of residue removal after compression and flex cycles. Ideal for CIP/SIP‑exposed elastomeric contact parts. Ensures compliance for polymer MoCs used in sterile and critical applications. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

UHMWPE – Full Cleaning Validation Description UHMWPE Cleaning Validation Coupons are designed to represent UHMWPE Cleaning Validation Coupons represent ultra-durable, abrasion-resistant polyethylene surfaces. They simulate chute liners, wear strips, guides and impact surfaces used in GMP utilities. UHMWPE offers very low friction and excellent chemical resistance, supporting accurate RF% studies. Its non-stick, low-energy surface requires validated residue recovery. Ideal for utilities exposed to high wear, impact, and repeated cleaning. Ensures polymer MoC compliance in validated cleaning programs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from UHMWPE. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for UHMWPE surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from UHMWPE ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: UHMWPE Cleaning Validation Coupons represent ultra-durable, abrasion-resistant polyethylene surfaces. They simulate chute liners, wear strips, guides and impact surfaces used in GMP utilities. UHMWPE offers very low friction and excellent chemical resistance, supporting accurate RF% studies. Its non-stick, low-energy surface requires validated residue recovery. Ideal for utilities exposed to high wear, impact, and repeated cleaning. Ensures polymer MoC compliance in validated cleaning programs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

Ultem – Full Cleaning Validation Description Ultem Cleaning Validation Coupons are designed to represent Ultem (Polyetherimide, PEI) Cleaning Validation Coupons represent high-temperature, high-strength engineering plastic surfaces. They simulate non-metallic components such as manifolds, housings, sensor blocks and structural parts. PEI offers excellent chemical resistance and dimensional stability under CIP/SIP conditions. These coupons enable RF% studies for high-performance polymer MoCs. Ultem’s low extractables profile suits regulated pharma and biotech systems. Ideal for validating cleaning on PEI-based contact and utility components.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from Ultem. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for Ultem surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from Ultem ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: Ultem (Polyetherimide, PEI) Cleaning Validation Coupons represent high-temperature, high-strength engineering plastic surfaces. They simulate non-metallic components such as manifolds, housings, sensor blocks and structural parts. PEI offers excellent chemical resistance and dimensional stability under CIP/SIP conditions. These coupons enable RF% studies for high-performance polymer MoCs. Ultem’s low extractables profile suits regulated pharma and biotech systems. Ideal for validating cleaning on PEI-based contact and utility components. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material

FKM/Viton – Full Cleaning Validation Description FKM/Viton Cleaning Validation Coupons are designed to represent FKM/Viton Cleaning Validation Coupons represent high‑performance fluorocarbon elastomer surfaces. They simulate chemical‑resistant gaskets, O‑rings, seals, valve seats and diaphragm components. FKM offers exceptional resistance to solvents, acids and high‑temperature cleaning agents. Its low‑swelling, non‑reactive behavior supports accurate RF% studies. Ideal for CIP/SIP‑exposed elastomeric components requiring robust cleaning validation. Ensures GMP compliance for fluorocarbon elastomer MoCs.. They are used in pharmaceutical, bioprocess, and GMP-regulated systems to assess residue recovery, detergent compatibility, and cleanability of equipment surfaces made from FKM/Viton. These coupons support RF% studies, swab and rinse recovery validation, and regulatory documentation for cleaning procedures involving this material of construction. ✔ KEY PURPOSES • Establish residue recovery factors (RF%) for FKM/Viton surfaces • Validate swab and rinse recovery in GMP cleaning procedures • Assess chemical compatibility with detergents and disinfectants • Provide FDA/EMA/PIC/S-compliant cleaning validation documentation • Ensure robust justification for equipment made from FKM/Viton ✔ MATERIAL CHARACTERISTICS • Material behaves as described in its summary: FKM/Viton Cleaning Validation Coupons represent high‑performance fluorocarbon elastomer surfaces. They simulate chemical‑resistant gaskets, O‑rings, seals, valve seats and diaphragm components. FKM offers exceptional resistance to solvents, acids and high‑temperature cleaning agents. Its low‑swelling, non‑reactive behavior supports accurate RF% studies. Ideal for CIP/SIP‑exposed elastomeric components requiring robust cleaning validation. Ensures GMP compliance for fluorocarbon elastomer MoCs. • Suitable for RF% reproducibility • Stable under standard cleaning conditions ✔ FORMATS • 50×50 mm or 75×75 mm validation plates • 2–5 mm construction depending on material