HSC Training

Advanced Training in Medical Device Registration and Market Authorisation
with International Certification

20-module training Live online delivery

Training modules

This advanced training programme brings together 20 strategic modules covering the full lifecycle of medical device registration, market authorisation and international certification. From structuring documentation to regulatory submission, including standards such as ISO 13485, ISO 14971, MDSAP and certification by ANVISA, FDA, CE and other authorities, this is the market's most comprehensive training for regulatory professionals seeking to master every stage with confidence and technical authority.

Medical Devices

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Develop your expertise in medical device registration, market authorisation and international certification with 20 comprehensive modules and accelerate your regulatory career.

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