BEST CONSULTANT FOR MEDICAL DEVICES AND PHARMACEUTICAL REGULATORY, CDSCO, ISO, CE, ISI, USFDA, MDSAP, 510k, TGA AUSTRALIA & QUALITY MANAGEMENT SYSTEM CERTIFICATION

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CE Marking

CE Marking, Free Sale Certificate & Medical Device registration with
European Regulatory Authority

CE Marking Certificate

Our professionals help your Organization to get CE Certificates for your Devices as per Medical Device Regulation 2017/745 and In-Vitro Medical Device Regulation 2017/746 and transition of MDD CE Certificate to MDR CE Certificate in shortest possible time and cost-effective way-

CE Marking for Medical Devices For Class I, Is, Im, Ir, IIa, IIb and III as per Medical Device Regulation 2017/745 and In-Vitro Medical Device Regulation 2017/746
Transition from MDD to MDR CE Certificate

Our professionals help you in

Designing Your Organization Infrastructure that Complies as per EU Directive / EU Regulation
Developing Complete Documentation Procedures
Assisting in Preparation of Technical Document for your Device
Identifying Tests required for your Device
Assisting in Finalization of EU Representative
Assisting in Selection of Appropriate Notified Body
Assisting in Getting CE certificate