Clean Room

Validation

Validation is done according to a predetermined validation protocol. Periodic validations in accordance with a maintenance and validation program tailored to the individual clean room class. In practice, this usually leads to a validation interval of 12 months of clean rooms with ISO class 6 or higher. For clean rooms with ISO class 5 or lower, the validation interval is usually 6 months. Reports are traceable and verifiable through our partner IETQAN web site. This way you will be able to share the report with regulatory agencies and clients with high credibility level.

The validation is done in accordance with ISO14644 

Our lab is accredited by EGAC   

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Roald Dahllaan 33 , 5629MC , Eindhoven , The Netherlands 

Whats-app +31685008887

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

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