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European Authorised Representative 

EU Responsible Person

UK Responsible Person

Medical Testing laboratory Services 

Lab Experiment

Package validation

Medical Devices Packaging System Validation as per ISO 11607

AT the LAb

Clean room validation

Validation Activities as per ISO 14644 requirements

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Residual EO/ECH Analysis

Testing activity as per ISO 10993-7

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Ethylene Oxide (EO) Sterilization Validation

Testing against the following standards 

Hemocompatibility testing ISO 10993-4

Cytotoxicity testing ISO 10993-5

Intracutaneous irritation testing ISO 10993-10

Sensitization testing ISO 10993-10

Systemic toxicity testing ISO 10993-11

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Packaging Accelerated Aging Studies

Packaging System Aging study as per ISO 11607 and following ASTM F1980

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Ethylene Oxide (EO) Sterilization Validation

Validation Activities as per ISO 11135 requirements and AAMI TIR 15 Read more >>

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European Authorized Representative (E.A.R.) serves as a legal entity designated by non European manufacturers to represent them in the EU and ensure their compliance with the European Directives/Regulations

Contact Us

Netherlands Office

Roald Dahllaan 33 , 5629MC , Eindhoven, Netherlands 

UK Office

7 Meeting Lane, Tibbets Close, Alcester, Warwickshire, United Kingdom, B49 5QU

Middle East Office 

Heliopolis , Nozha Gedida , Cairo m Egypt , 11 Ahmed Makhmer St. 

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Whats-app +31685008887

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© Copyright. EUCEREP 2021

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