Blogs
Medical Devices–USA/Europe Regulatory…
EUROPE
MDCG 2022-14 – Transition to the MDR and IVDR – Notified body capacity and availability of …
USA/Canada/UK/EU approved product Lab…
Below are some analytics and counts of Product labels released from Canada, USA, UK and EU. Following…
Color Additive Petitions
FDA Recommendations for Submission of Chemical and Technological Data on Color Additives for Food, Dr…
Medical Devices – USA/Europe Regulato…
EUROPE Commission Implementing Regulation (EU) 2021/2226 of 14 December 2021 laying down rules for t…
MHRA Guidance on the use of Real-Worl…
There are vast amounts of data being collected on patients, for example, in electronic health records…
Procedural Aspects for the Consultati…
The guidance document aims to provide interested parties in particular notified bodies, device manufa…
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