News and Insights

Case Study: MHRA GMP Mock Inspection for a Client in APEC

Introduction: The client, a leading pharmaceutical company based in the APEC region, recently successfully passed a rigorous PIC/S...

**Driving Pharmaceutical Excellence Across Borders: The Inviva Success Story*

At Inviva, we take pride in our commitment to facilitating global partnerships and driving pharmaceutical excellence across international...

Empowering Global Access: The Inviva UKRP Consultancy Success Story

At Inviva, we are committed to empowering global access to medical device products by providing comprehensive consultancy services...

Update on the use of AI in medical devices in Europe

The first 6 months of 2023 have seen Artificial Intelligence or ‘AI’ become inserted into everyday vocabulary, with the media trying to...

Medical Device News – the latest on UKCA mark and plans to reform UK regulation

You could say it has been a challenging few years for medical device and in vitro diagnostic manufacturers in the UK and EU when it comes...

UK MHRA plans to fast-track cutting edge medicines

This week, the UK Government announced its spring budget, with a £10m package awarded to the Medicines and Healthcare products Regulatory...

EC proposal for revised EU MDR and IVDR transition periods

Not for the first time since the introduction of the Medical Device Regulation (EU) 2017/745 and its IVDR (EU) 2017/746 sibling, we see...