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...
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.
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...
The Story Behind Braid: How the Brand Reflects Advarra’s Vision for Data and AI in Clinical Research
Estimated reading time: 6 minutes Advarra partnered with PreHealth, a brand growth and experience...
Are you prepared for ICH E6 (R3)?
The third revision (R3) of the ICH E6 Guideline for Good Clinical Practice represents...
The Executive Order that Brings Private Bioresearch Under Federal Oversight
The release of ICH E6(R3) in January 2025 marks the most significant evolution in...
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