Sponsor’s Guide to IRB Approval: What Every Sponsor Needs to Know Before Submitting a Study
Introducing the “‘Sponsor’s Guide to IRB Approval’” Institutional review board (IRB) approval protects the rights, safety,...
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 Director of Training in IRB Services Lori Young
Lori Young has spent her career at the intersection of research, ethics, and education—and...
Q&A with Advarra’s Senior Coordinator of Client Services Jani Viox
For Jani Viox, clinical research is more than a profession—it’s personal. As a senior coordinator...
How Smarter Clinical Trial Study Design Decisions Set Studies Up for Faster Startup and Fewer Amendments
Estimated reading time: 8 minutes Clinical trial study design forms the foundation of trial...
Why Research Sites Are Switching to Connected eISF and CTMS
Estimated reading time: 4 minutes Fueled by automation to remove one of the biggest...
New Paper Makes the Case for AI-Specific Guidance in Research Oversight
Estimated reading time: 3 minutes AI is becoming a routine part of how research...
Reducing Startup Delays in Oncology Clinical Trials Through Consistent IRB Processes
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
What Are the Different Types of Study Designs?
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
Q&A with Senior Manager of Client Services Francine Lopez
Estimated reading time: 3 minutes For nearly a decade, Francine Lopez has helped clinical...
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