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Ensure your medical devices meet European standards with CE Marking. Stay compliant and gain market access across the EU. Maven is a regulatory consultancy providing one-stop solution for the CE marking of your medical devices, providing overall support with technical documentation, identification of external testing and coordination with associate laboratory partners, generating UDI’s, EUDAMED registration, appointment of EC REP (European Authorised Representative) and coordination with notified body.
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Punyam.com offer CE Mark consultancy in India. CE Marking is a declaration by a manufacturer that their product meets all relevant provisions of Europ...
India’s healthcare market is expanding rapidly, offering tremendous opportunities for manufacturers and importers of medical devices. However, before ...
Unlock Global Compliance for Your Medical Device Portfolio Are you navigating complex regulatory landscapes for medical devices—whether high-risk impl...
We have experienced ISO 13485 consultants that can help your medical device manufacturer become compliant with the latest industry standards.ISO 13485...
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