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White Papers, Case Studies, Reports

Use case: Implementing digital solutions to improve oncology trial experience & efficiency

A top 10 pharmaceutical company looked to Medable to streamline participant burden and enhance site and team experience in oncology trials, while establishing a scalable template for future trials in oncology and other areas.

Webinars

What it really takes to adopt eConsent across large pharma

Learn about the benefits of adopting consent management technology and best practices around developing change management and training programs to help sponsors, CROs and sites get the most out of eConsent.

Blog posts

What does the new European Medicine Regulatory Network recommendation paper on decentralized elements in clinical trials tell us?

Learn what impacts the new European Medicine Regulatory Network recommendations paper means to your clinical trial operations.

Blog posts

New EU Regulatory Recommendations for Decentralized Trials Keep Focus on Patients and Sites

As clinical trials rapidly modernize, government regulators work to evolve even as the same core principles apply. Still, decentralized clinical trials are – simply – clinical trials, as all research today is decentralized in some way, yet we lack global harmonization of regulations.

Blog posts

J.P. Morgan Week 2023: Trends, highlights, and themes from this year’s conference

See what key trends and takeaways were at the 2023 JPM conference and how they'll drive the landscape of pharma.

Webinars

Building trust between clinical trial stakeholders through a DCT framework

Industry experts from Pfizer, Advarra, and Medable showcase how to design a framework of decentralized offerings that provide greater ease of use, effectiveness, and flexibility for sites for every type of research setting; decentralized/hybrid, virtual, or in-person. In addition, they discuss how DCT solutions and site partners are creating an impact to improve diversity and access while optimizing clinical research for patients.

See how Medable can make your trials more efficient.