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Certifications

Certifications

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ISO 13485 for the manufacture of medical devices

ISO 13485 certification ensures that the quality management system complies with the requirements of medical device standards. ISO 13485 is the medical device industry standard for quality management and adoption can help standardise and systematise the medical device development process. Once adopted, ISO 13485 can simplify processes. With the entry into force of the new MDR, ISO 13485 certification has become indispensable for both manufacturing companies and companies marketing MDs.
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ISO 22716 Cosmetic GMP

This is the harmonised standard that describes the GMP (Good Manufacturing Practice) requirements specific to the cosmetics sector. The purpose of the standard is to demonstrate compliance with Good Manufacturing Practice (GMP) to ensure quality and to meet the requirements of the new Cosmetics Regulation.
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