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Blog & Articles related to Medtech - Page 2

Europe Regulation

Blog & Article

European Commission proposes conditional extension of IVDR requirements

11th March 2024

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Blog & Article

FDA takes steps to harmonize medical device QMS requirements

7th March 2024

Blog & Article

Hong Kong paves the way for mandatory regulatory framework for medical devices

13th February 2024

Blog & Article

Preparing for device tracking: Next steps with Australia’s UDI

16th November 2023

Blog & Article

Understand Implications of Latest Amendment to MDR and IVDR published in March 2023

23rd August 2023

FDA Blog

Blog & Article

FDA starts 2023 with a flurry of guidance documents

24th July 2023

Blog & Article

ARCS Takeaways: IVDR in an Australian Context

17th July 2023

Blog & Article

TGA updates its reclassification timelines

11th July 2023

Blog & Article

Regulation of Personalized Medical Devices in Australia

4th July 2023

Blog & Article

Key takeaways from 2023 Euro Convergence

16th June 2023

Blog & Article

The importance of performance studies for IVDs

15th June 2023

Blog & Article

What is a PRRC and why is it necessary for medical device manufacturers to have one?

30th May 2023

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