Blogs

October 26, 2022 | Medical Device

Adverse incidents involving medical devices that occur in the UK must be reported to the Medicines an…

September 27, 2022 | Medical Device

EUROPE MDCG 2022-14 – Transition to the MDR and IVDR – Notified body capacity and availability of …

September 27, 2022 | Standards

Below are some analytics and counts of Product labels released from Canada, USA, UK and EU. Following…

September 24, 2022 | Standards

FDA Recommendations for Submission of Chemical and Technological Data on Color Additives for Food, Dr…

January 11, 2022 | Medical Device

EUROPE Commission Implementing Regulation (EU) 2021/2226 of 14 December 2021 laying down rules for t…

January 7, 2022 | Standards

There are vast amounts of data being collected on patients, for example, in electronic health records…

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