News & Insights

An expert holding a microphone gives a talk about in vitro diagnostic clinical trials to an interested audience.
 
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Our industry is constantly evolving, from in vitro diagnostic (IVD) advances and New regulatory requirements to Emerging Technologies and clinical trial best practices. Get an expert perspective from Beaufort.

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Considerations for Sponsors Navigating a Shifting Landscape Read more
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Authored By: Beaufort Contributor On 27 November 2025, the European Commission published Commission Decision (EU) 2025/2371, formally confirming that the first four modules of EUDAMED—Actor Registration, ... Read more
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EU and U.S. Regulatory Considerations for Post-Market Advertising and Promotion of IVDs Authorized in vitro diagnostic medical device (IVD) claims must be supported by a defined ... Read more
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Authored by: Beaufort Contributor The AMDM IVD Focus Fall Meeting brought together regulators, industry leaders, and diagnostic professionals for two days of focused discussion and actionable ... Read more
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MedTech Clinical Trial Readiness eBook Read more
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Point-of-Care (POC) diagnostic trials for influenza are unlike any other. The season is short, virus circulation is unpredictable, and enrollment targets — particularly for influenza B ... Read more
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What It Means for FDA Operations and the Diagnostics Industry Authored by: Beaufort Contributor When the federal government shut down on October 1, 2025, the U.S. ... Read more
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Insights from the IVD Track at MedTech Summit 2025 The IVD track at MedTech Summit 2025 in Berlin brought together regulators, notified bodies, and industry experts ... Read more
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Authored by: Beaufort Contributor From MDUFA to EUDAMED—What Regulatory Leaders Need to Know The 2025 AMDM Annual In Vitro Diagnostics (IVD) Regulatory Meeting delivered two full ... Read more
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Updates to the UK Medical Device Regulations Authored by: Beaufort Contributor The regulatory landscape for medical devices, including in vitro diagnostics (IVDs), in the United Kingdom ... Read more
ANNOUNCEMENT
Strengthening our Commitment to Successful Client Outcomes Nilufer Celenk, Vice President, Clinical Program Management Beaufort is excited to welcome Nilufer Celenk, as Vice President of Clinical ... Read more
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Key Changes and Implications for Interventional Clinical Trials Authored by: Beaufort Contributor On January 6, 2025, the International Council for Harmonisation (ICH) officially released (adopted) the ... Read more
 
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Beaufort is pleased to sponsor AMDM’s Fall IVD Focus Meeting. Come meet our team from Oct 17-18 in … Read more

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On Aug 20, Beaufort is presenting “Clinical Trials with CDx—Navigating the Complexity of the IVDR” at the … Read more

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Visit Beaufort in Booth # 4739 at the ADLM 2024 Annual Meeting in Chicago (July 30 – Aug 1). Set a meeting with our experts.… Read more

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Beaufort will be presenting “Exploring the CDx Landscape” at the 17th Annual IVD Clinical and Regulatory Affair … Read more

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Visit our team during AMDM’s 50th Annual IVD Regulatory Meeting & FDA IVD Submission Workshop from April 22-25, 2024.… Read more

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Visit our team in booth #201 at Precision Med TRI-CON from 3/26 – 28 in San Diego … Read more

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Beaufort is attending SCOPE Summit. Let’s meet to discuss your clinical monitoring oversight needs. … Read more

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Beaufort is pleased to be a conference sponsor of MedTech Summit in Brussels, Belgium from June 19 – 23. Our SVP, Global … Read more