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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...
Paisely
Jun 21, 20242 min read


**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...
Paisely
Mar 13, 20242 min read


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...
Paisely
Mar 5, 20242 min read


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...
Bryan Lister
Jul 28, 20232 min read


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...
Bryan Lister
May 23, 20232 min read


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...
Bryan Lister
Mar 20, 20231 min read


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...
Bryan Lister
Mar 18, 20232 min read
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