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Our insights overview

12 January 2022

New regulation | eIFU

28 May 2021

The EU’s Medical Device Regulation (MDR) went into force

23 November 2020

Webinar: MD development deliverables needed for NoBo submission under MDR

4 November 2020

The what, how, why and when of a post-market surveillance system

1 October 2020

IEC 60601 just got amended

28 August 2020

Is my wheelbarrow a Machine?

24 July 2020

ISO 14971 third edition: what’s new?

24 April 2020

MDR postponed with 1 year

25 March 2020

Active medical device: which sterilization method to use?

23 September 2019

Anti-microbial coatings for medical devices under MDR

23 August 2019

Traceability: track your device globally using UDI

5 July 2019

Duly justified

29 May 2019

Unitron Regulatory workshop on Medical Device modifications

22 March 2019

We have received our renewed QMS certificate

22 March 2019

MDR: is your company ready?