In this free webinar, understand the key benefits of master protocols. Attendees will identify the key challenges of master protocols and strategies to address them. The featured speakers will discuss ...

At this year's conference, TransCelerate and representatives from its member companies, including Amgen, Merck, and Pfizer, will participate in seven sessions addressing topics such as data collection ...

Delivered jointly by 4G Clinical, Converge and a sponsor representative, this session brings together the operational viewpoints that most directly shape trial readiness, offering attendees a grounded ...

Citeline’s Best-in-Class Data and AI Combine with Risklick’s End-to-End Digital Protocol Workflow Suzanne Caruso Suzanne Caruso, Citeline Poorya Amini Dr. Poorya Amini, Risklick NEW YORK, Jan. 13, ...

A clinical trial protocol is the foundation of clinical research, detailing objectives, study design, eligibility, safety oversight, and data analysis. Its structure ensures consistency and ...

Successful clinical trial conduct balances participant safety, treatment efficacy and operational feasibility. But slow patient identification and enrollment, cost overruns and missed deadlines pose a ...

Adaptive clinical trial design represents a modern approach to evaluating healthcare interventions that allows pre‐specified modifications based on accumulating data. This flexible methodology ...

As the curtain closed on 2024, FDA issued a new draft guidance to assist clinical trial sponsors, investigators, and institutional review boards (“IRBs”) with defining, identifying, and reporting ...

The U.S. Food and Drug Administration (FDA) published the draft guidance “Protocol Deviations for Clinical Investigations of Drugs, Biological Products, and Devices,” which provides advice for ...

(MENAFN- GlobeNewsWire - Nasdaq) Citeline's Best-in-Class Data and AI Combine with Risklick's End-to-End Digital Protocol Workflow NEW YORK, Jan. 13, 2026 (GLOBE NEWSWIRE) -- Citeline, a leader in ...