Understanding how to Build and Leverage a DSMB Statistical Plan
Discover the DSMB statistician’s critical role in safety monitoring, including SAPs, validated programming, and study design impact on analysis.
How to Optimize Your sIRB Experience
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Rare and Orphan Diseases in Regulated Development
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Analyzing 1,000+ Study Startup Records for Recruitment Performance with Advarra Study Collaboration solutions
Our team investigated Advarra study collaboration solutions (Advarra Study Startup and Advarra Enroll) impact on site’s ability to reach recruitment goals on time – regardless of sponsor or therapeutic area. Download the case study to learn more.
Top Biotech Achieves Recruitment and Improves Compliance Across 30 Sites
Download the case study to find out how the Advarra’s study collaboration solutions ensured not only recruitment success, but site and participant support and compliance.
Budget Negotiation 101
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Setting Yourself up for Success During Investigator-initiated Trials
This eBook outlines Tips and best practices for a successful IIT, Post-approval monitoring and clinical project, and Leveraging industry sponsors.
Yale Enhances Patient Safety, Billing Workflows with OnCore and EMR Integration
Discover how Yale, Advarra, and Epic improved billing compliance, streamlined workflows, and enhanced participant safety through OnCore-EMR integration.
Site Streamlines Operations with Advarra EDC Study Design Service
Learn how a major cancer center streamlined operations with Advarra’s EDC Study Design Service, improving eCRF builds and reporting efficiency.
Onboarding & Training for Clinical Research Professionals
In this webinar, Miranda Schramm, Director of Training at Advarra, covers strategies for new hires joining the clinical trial industry.
Rare and Orphan Diseases: Choosing a Path to Regulatory Approval and Market Success
Explore regulatory pathways and strategies for bringing rare disease therapies to market, addressing challenges in drug development and pricing.
What Does an Endpoint Adjudication Committee (EAC) Do?
Learn how Endpoint Adjudication Committees ensure safe study conduct, mitigate participant risks, and provide unbiased medical event reviews.