Q&A with Advarra’s new Senior Vice President, FDA Regulatory Advisor, Jan Hewett
Clinical research drives medical progress. Advarra ensures participant safety and ethical standards through expert...
FEATURED E-BOOK
Making Good Clinical Practice More Understandable
This eBook dives into GCP’s role in the clinical research ecosystem and how it protects participant rights, safety, and confidentiality.
The Value of Clinical Research
Clinical research drives medical progress. Advarra ensures participant safety and ethical standards through expert...
Advancing and Safeguarding Clinical Research for a Better Tomorrow
Advarra's commitment to ethical clinical research for over 35 years drives medical breakthroughs, ensuring...
An Interview with Jim Kremidas: What’s Next for the Association of Multisite Research Corporations (AMRC)
Launched in January 2025, the Association of Multisite Research Corporations (AMRC) was set up...
Help for HRPPs: Educating the New Researcher community on SBER Basics
The beginning of a new semester brings a fresh crop of aspiring researchers to...
Ways to Streamline Informed Consent Process in Clinical Trial Startup
Estimated reading time: 5 minutes At a busy research site, a clinical trial is...
2025: Perspectives and Predictions From Advarra Thought Leaders
2024 has been a year of growth and evolution in clinical research. The coming...
Choosing Your Electronic IRB System: A Guide for Sites
Selecting an electronic institutional review board (eIRB) system is a critical decision for institutions...
The Importance of a Large Network of KOLs for DMCs
In the complex landscape of clinical trials, the data monitoring committee (DMC) serves as...
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