10 Clinical Trial Regulatory Changes Coming in 2025
Clinical trials are changing fast. New technologies, stricter data requirements, and pressure to speed up drug development are reshaping how we run studies. Here’s what
June 24, 2025
YORIK DRAFT – EMA IDMP Roadmap: Updates, Requirements and Impact on Industry (Session 1 of 2)
By the end of 2024, EMA updated the IDMP guidance and the Product Management Service (PMS) implementation guide after the achievement of some milestones including
May 21, 2025
Open Label Study
A type of study in which both the health providers and the patients are aware of the drug or treatment being given. Source: NCI
August 31, 2022
Sponsor Oversight and the Role of eTMF | Webinar
Clinical Webinar Sponsor Oversight and the Role of eTMF Learn how your industry colleagues are conducting TMF oversight and overcoming common challenges. Wednesday, July 20,
July 7, 2022
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