Regulatory Check-up France

Is your company based in France? 🇫🇷 Do you have questions about the MDR, IVDR, ISO 13485, MDSAP, or other Regulatory, Quality and Clinical topics? Don’t miss this chance to have a private, 1-hour session where our experts answer all your questions.

Places are limited, register now!

Grounding Your Medical Device Investment in a Foundational Needs Assessment

We sat down with leaders from top life sciences companies to discuss foundational needs assessments – how to do them, what can go wrong when you...

Read More
Event Recap: Biocompatibility Insights 2023

1 min read

Event Recap: Biocompatibility Insights 2023

This year’s Biocompatibility Insights conference took place in Annapolis, MD, US from September 25–27, 2023. The framework for the event was...

Read More
Artificial Intelligence (AI), General Data Protection Regulation (GDPR) and Cybersecurity: 10 Misconceptions About Medical Device Software

Artificial Intelligence (AI), General Data Protection Regulation (GDPR) and Cybersecurity: 10 Misconceptions About Medical Device Software

Medical Device Software (MDSW) is a growing, fast-evolving industry. However, manufacturers must often face a regulatory framework which does...

Read More