Identifying Risks in a Tidal Wave of Clinical Trial Data
Reading Time: 3 minutesThe rising complexity of clinical trials has created… Read More
Building a 360° View of the Patient Experience by Using a Unified Clinical Data Management Platform
Reading Time: 4 minutesClinical trials have evolved rapidly over recent years. They now have… Read More
Medidata Detect and eCOA in Decentralized Clinical Trials
Reading Time: 2 minutesWhile decentralized clinical trials (DCTs) have provided benefits for participants such as fewer… Read More
Women in Clinical Trials for Biomedical Research | Medidata’s Diversity in Clinical Trials Series
Reading Time: 3 minutesThis blog was authored by Fiona Maini, Global Compliance and Strategy principal, Medidata,… Read More
External Control Arms in Clinical Trials | MIT Technology Review & Medidata Solutions
Reading Time: 2 minutesWritten in partnership… Read More
What’s Next for External Controls | MIT Technology Review & Medidata Solutions
Reading Time: 2 minutesWritten in partnership with MIT Technology Review External control arms… Read More
How Mid-sized & Emerging Biopharma Sponsors Can Choose Clinical Trial Technology For Their Needs
Reading Time: 3 minutesInsights from Medidata Experts Mid-sized and emerging biopharma companies drive innovation in… Read More
How Mid-sized Biopharma Sponsors Can Leverage Medidata’s Clinical Trial Technology and Expertise
Reading Time: 3 minutesInsights from Medidata Experts Mid-sized and emerging biopharma companies drive innovation in… Read More
What My Experience in a COVID-19 Vaccine Trial Taught Me About the Need for Greater Patient Centricity
Reading Time: 5 minutesKelly McKee, Vice President of Patient Registries and Recruitment at Medidata, recently participated… Read More
FDA Approval in External Control Arms | MIT Technology Review & Medidata Solutions
Reading Time: 3 minutesWritten in partnership with MIT Technology Review How does the U.S. Food… Read More
