•CE Mark & CE Marking Technical File Preparation
Medical device quality & regulatory consultants for Technical File construction, CE Marking, ISO 13485:2003, GMP, FDA compliance, 510k, ISO 14971 & EU Authorized Representative for Europe.
•Dansk Standard - Establishing Compliance with the Medical Devi...
The course is designed to give you an understanding of the requirements of the Medical Device Directive (MDD 93/42/EEC). At the end of the course, you will be able to implement the requirements of the Directive and to audit organi...
•Life Sciences | IIR Conferences
Informa Life Sciences is dedicated to serving the information needs of the global Life Sciences community. Our acclaimed portfolio of conferences, exhibitions and seminars ensure that you will be kept up to date with the latest te...
•Dansk Standard - Course - Compliance with the Medical Device D...
The course is designed to give you an understanding of the requirements of the Medical Device Directive (MDD 93/42/EEC). At the end of the course, you will be able to implement the requirements of the Directive and to audit organi...
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