Blog
FDA Letter to Industry Calls on Device Sponsors to Independently Verify Third-Party Data
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Blog
At-Home, POC, DCTs & Hybrid Models: IVD Expertise Across Every Use Setting
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Blog
Regulatory Insights to Meet Evolving IVD QMS Requirements: LDTs, IVDR, & QSR to ISO 13485:2016
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Article
Unlocking Technology: The Advantages of a Tech-Savvy CRO for IVD and Device Trials
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Blog
Navigating the Future of Clinical Trial Monitoring
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Article
The Keys to Effective Sample Management for IVD Clinical Studies
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Article
How Intended User and Use Setting Impact Study Design and Regulatory Requirements
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Blog
The potential impact of the EU Commissions proposal to delay IVDR implementation
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