News & Insights

An expert holding a microphone gives a talk about in vitro diagnostic clinical trials to an interested audience.
 
All Thought Leadership

Our industry is constantly evolving, from in vitro diagnostic (IVD) advances to regulatory requirements to clinical trial best practices. Get an expert perspective from Beaufort.

 
Blog

FDA Letter to Industry Calls on Device Sponsors to Independently Verify Third-Party Data … Read more

Blog

At-Home, POC, DCTs & Hybrid Models: IVD Expertise Across Every Use Setting … Read more

Blog

Regulatory Insights to Meet Evolving IVD QMS Requirements: LDTs, IVDR, & QSR to ISO 13485:2016 … Read more

Article

Unlocking Technology:  The Advantages of a Tech-Savvy CRO for IVD and Device Trials … Read more

Blog

Navigating the Future of Clinical Trial Monitoring … Read more

Article

The Keys to Effective Sample Management for IVD Clinical Studies … Read more

Article

How Intended User and Use Setting Impact Study Design and Regulatory Requirements … Read more

Blog

The potential impact of the EU Commissions proposal to delay IVDR implementation … Read more