RESOURCES AND INTELLIGENCE

FOR MEDICAL DEVICE REGULATORY PROFESSIONALS

QFI offers a wide range of articles, discussion papers, guidance, contributions and other resources on international medical device regulation, including EU Regulation, US Regulation, Standards, Quality, Microbiology and many more.

To order any of these publications, please send an email to [email protected].

QFI offers assistance to medical device companies affected by LRQA’s cessation of Notified Body services under the Medical Devices Directives

Jun19
London-based medical device regulatory consultancy Quality First London-based medical device regulatory consultancy Quality First International offers medical device manufacturers support on this matter, including transitions to another Notified Body. The British medical device regulatory consultancy

Out now: A handy guide provides quick and simple insight into the world of medical device standards

Feb11
London-based medical device regulatory consultancy Quality First International has written a basic guide to the use of standards to demonstrate fulfilment of product specification, conformity with European regulations or specified requirements of medical devices. Haroon

Quality First International launches post-Brexit UK Responsible Person Programme for medical device manufacturers

Feb19
London-based medical device regulatory consultancy Quality First International now offers post-Brexit UK representation services that will become mandatory for medical device manufacturers located outside the UK. The British medical device regulatory consultancy Quality First International

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