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      20th November 2025
      
      Good Morning Meeting – 18 September 2025 – Copenhagen, Denmark
      
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Blog & Articles related to Medtech - Page 3

Blog & Article

TGA’s updates and key changes in the MDR transition strategy

22nd May 2023

Blog & Article

How tighter rules modernize and safeguard India’s medical devices market

13th April 2023

Ciber security

Blog & Article

Navigating AI and cybersecurity in the rapidly evolving world of SaMDs

5th April 2023

Medical Devicces Regulation (EU) 2017/745

Blog & Article

Common Specifications for medical devices without an intended medical purpose

20th February 2023

Blog & Article

Why pre-submission meetings benefit medical device manufacturers

13th February 2023

In Vitro EU regulation

Blog & Article

Countdown for EU health institutions using in-house devices

30th January 2023

IVDR technical files

Blog & Article

Making technical files clear, concise and easy to navigate is key under IVDR

14th December 2022

FDA Chemical Risk Assessment Tools

Blog & Article

FDA Publishes Chemical Risk Assessment Tools (CHRIS)

7th December 2022

Bio Ateliar Take aways

Blog & Article

Biotech Atelier – Innovation and Regulations September 28, 2022

30th November 2022

Europe Regulation

Blog & Article

The challenge of finding and working with a Notified Body under the IVDR

28th November 2022

UK MedTech Regulation

Blog & Article

MHRA updates on the future UK Medical Device Regulation

31st October 2022

Medical Devices Tenders Hong Kong

Blog & Article

New government tender requirement for medical devices in Hong Kong – Revised version 06/14/2023

26th October 2022

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