Upcoming Webinars
Re-Air: Faster Trials, Successful Sites, Empowered Patients: Improve Your Research Experience
March 21, 2024 | 12 pm GMT | 1 pm CET
Optimize clinical trials with practical solutions, real site feedback, and tools for seamless success. Join our webinar to revolutionize your research approach.
Read moreNavigating sIRB Complexities: An Interactive Session
March 26, 2024 | 1 pm ET
Join us as we share insights, strategic priorities, and guidance for preparing your institution for sIRB mandates.
Re-Air: DSMB Best Practices and Behind the Scenes Insights
March 28, 2024 | 12:00 pm GMT | 1:00 pm CET
Enhance clinical trial oversight with expert insights on member selection, bias elimination, and regulatory compliance from 20+ years of leadership experience.
Striking the Balance: Ethics, Inclusion, and Vulnerability in Research
April 2, 2024 | 1 pm ET
Explore the ethical tensions between including under-represented communities and ensuring vulnerable participant populations are appropriately protected.
Inside Study Activation: Budgeting Takeaways
April 18, 2024 | 1 pm ET
Learn how sites, sponsors, and CROs can work together to help study activation, specifically within budgeting and contracting.
On-Demand Webinars
Have a question about our webinars? Check out the Webinar FAQ.Learn a comprehensive overview to prepare sponsors and sites for an FDA inspection.
There is great potential for research surrounding rare diseases. Uncover various types of gene delivery and its impact on diverse populations in the U.S.
Explore IRB considerations for overcoming study enrollment barriers while ensuring risks to participants are appropriately minimized.
Leverage best practices for IRB review of decentralized trial elements sourced from research community experts.
Explore strategies for sponsors and CROs for implementing an enterprise phased QMS assessment, and address deficiencies in compliance and implement corrective actions.
Learn the basics of working with an sIRB and gain insights for successful sIRB relationships with external IRB partners.
Discover strategies for proactively assessing compliance for an FDA Inspection Readiness visit. Address deficiencies and implement corrective actions.
Join us as Advarra experts outline how sponsor organizations can work with various site types across trials and adapt their resources accordingly.
Gain an understanding of what an eReg system is and the features available to streamline clinical trial regulatory management.
Learn strategies to streamline workflows across sites and sponsors, and explore success stories on how to reduce site burden.