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Top 10 Clinical Trial Trends for 2024

XTalks

From the continuing trend of the rapid adoption of AI tools to the growing use of real-world evidence (RWE) in regulatory decision-making and a focus on enhancing data integrity, find out how clinical trials will evolve in 2024 to shape the future of medical research. percent from 2023 to 2033.

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Can technology help diversify clinical trials?

pharmaphorum

This is the second in a two-part series examining how pharma can embrace the DEI agenda to create more effective medicines through more representative clinical trials. The same principles are increasingly being applied to clinical trials to improve diversity, mitigate bias, and reinforce inclusion in clinical trials.

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Clinical Data Management Experts Share Insights on Modern Digital Clinical Trials

XTalks

In this interview, Xtalks spoke with experts from eClinical Solutions , Katrina Rice, Chief Delivery Officer, Data Services; and Diane Lacroix, Vice President, Clinical Data Management, about clinical data management for modern day digital clinical trials. Data security: The clinical trial data is backed-up and secure.

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2022 in review: Regulation starts to catch up with AI in pharma

Pharmaceutical Technology

This is true not only in the case of the general public using applications for creating images or text, but also for pharma companies to improve drug discovery, clinical trial recruitment, and finding new biomarkers. Other companies have chosen to expand upon previous partnerships with AI giants.

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Decentralised identities: Blockchain based informed consent

Drug Discovery World

Industry experts explain how blockchain can fundamentally enhance clinical trials. Obtaining consent from patients or healthy volunteers is a fundamental requirement for enrolling participants on to clinical trials. for clinical trial participants. for sponsors or sites, or private, eg.

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Decentralised identities: Blockchain based informed consent

Drug Discovery World

Industry experts explain how blockchain can fundamentally enhance clinical trials. Obtaining consent from patients or healthy volunteers is a fundamental requirement for enrolling participants on to clinical trials. for clinical trial participants. Informed consent in the future.

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Safeguarding Patients: A Day in the Life of a Pharmacovigilance Leader

XTalks

Over the years, his career has evolved from routine case processing at large pharma companies to a more strategic role in smaller settings, where he feels his impact more directly. Collaboration: The Key to Success The essence of pharmacovigilance at small companies according to Ashish, lies in teamwork.