Standards by Industry Sector

Packaging for terminally sterilised medical devices - Part 1 : Requirements for materials, steri...

Packaging for terminally sterilised medical devices – Part 2 : Validation requirements for formi...

Medical devices — Quality management systems — Requirements for regulatory purposes

Clinical investigation of medical devices for human subjects — Good clinical practice

Medical devices — Application of risk management to medical devices

Medical devices — Symbols to be used with medical device labels, labelling and information

Medical devices – Symbols to be used with information to be supplied by the manufacturer – Part ...

Medical devices — Guidance on the application of ISO 14971

Medical devices – Part 1 : Application of usability engineering to medical devices