How Sponsors Can Use Adaptive and Platform Trial Models to Reduce Amendments and Accelerate Study Start-Up
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
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.
Q&A with Advarra’s Client Experience Partner Brian Boggs
Estimated reading time: 3 minutes As a member of Advarra’s client experience team, Brian...
Enabling Oncology Site Success: Tackling the Barriers That Slow Cancer Research
Estimated reading time: 8 minutes Oncology clinical trials are becoming increasingly complex, placing new...
Q&A with Advarra’s Associate Director of Client Services Anna Carnevale
Estimated reading time: 3 minutes Over the past 14 years, Anna Carnevale, associate director...
Building Customer Experiences That Lead to More Hope for Patients
Estimated reading time: 4 minutes Clinical research gives people hope. For some, it’s the...
Clinical Trial Budget Negotiations: A View From Each Side
Budget negotiation success hinges on clear communication and early resource sharing, helping sites and...
The Impact of ICH E6(R3) on U.S. and Canadian IRBs
Now that FDA has published the ICH E6(R3) Good Clinical Practice (GCP) guidance, aligning...
Medicare Coverage Analysis Worksheet
Medicare Coverage Analysis outlines criteria to determine coverage eligibility, guiding trials through compliance with...
Advarra’s Perspective on FDA’s Draft AI Guidance: Advancing Responsible Innovation
Estimated reading time: 4 minutes The U.S. Food and Drug Administration’s (FDA’s) recent draft...
Looking for More?
To register for upcoming webinars and see where we’ll be next, go to the Events page.
Want to see the latest news and updates about Advarra? You can find them in the Newsroom.
