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      Blog & Article
      
      25th April 2024
      
      Centralize, Modernize, Harmonize: The Acceleration of Regulatory Digital Trends
      
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      27th March 2024
      
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Blog & Articles related to Medtech - Page 3

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

MedTech Blog

Blog & Article

TGA to recognise medical device evidence from Singapore

28th September 2022

toxicology

Blog & Article

How integrated product development can transform an ATMP program

1st September 2022

MDR_blog

Blog & Article

Understanding the changing roles of economic operators under the MDR

23rd August 2022

medical device

Blog & Article

Why going above and beyond with PMS is key to supporting medical devices

16th August 2022

Blog & Article

Navigating the impact of the IVDR on marketed products

24th March 2022

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Strategic and Scientific Consultancy
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Innovations to Market
Post-launch Outsourcing
Local Affiliate Services
Business and Portfolio Mergers & Acquisitions

Strategic and Scientific Consultancy
Integrated Product Development
Innovations to Market
Post-launch Outsourcing
Local Affiliate Services
Business and Portfolio Mergers & Acquisitions

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