On-demand Webinar

Current State of Site-Sponsor-CRO Collaboration

Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing even…

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Balancing Innovation, Ethics, and Operational Excellence in Adaptive Oncology Trials

Balancing Innovation, Ethics, and Operational Excellence in Adaptive Oncology Trials Clinical trials are evolving to…

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Demystifying North American IRB/EC Requirements for International Research Professionals

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Not if, but When: A Study Manager’s Guide to Adaptability and Incoming Trends

Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing even…

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Reducing Site Burden Throughout Study Startup

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Overseeing and Operationalizing Patient Recruitment Across Study Stakeholders

This webinar will tackle the most pressing challenge in clinical research: achieving enrollment targets on…

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Unlocking Global Potential: Partnering Across Varying Sites in Study Startup

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Fireside Chat: The Future of Clinical Trials and Site Engagement

Learn about the challenges sites face and see how sponsors and CROs can work more…

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Advantages and Considerations for an eRegulatory Implementation

Learn best practices for eRegulatory (eReg) systems, and hear tips for academic medical centers, cancer…

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How Your Study’s Informed Consent Can Help Simplify Study Startup

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Simple Ways to Uncover Research Compliance Blind Spots

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Adapting to the Evolving Era of Oncology: Implications and Strategies for Research Institutions

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Building Buy-in: Strategic Training for Clinical Research Success

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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From Simulation to Success: Stress Testing Your Inspection Readiness

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Decentralized Clinical Trials Involving Biologics: Unique Challenges

Join this webinar to learn about FDA insights on DCTs and biologics. Dr. Eisenman discusses…

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Medicare Coverage Analysis in Oncology Trials

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Preparing Your Action Plan for the FDA sIRB Mandate

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Business Best Practices for Research Sites Webinar

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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The Importance of Strategic Planning for Long-term Training Success

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Inside Study Activation: Budgeting Takeaways

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Striking the Balance: Ethics, Inclusion, and Vulnerability in Research

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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DSMB Best Practices and Behind the Scenes Insights

Ensure your DSMB meets regulatory standards. Learn best practices in administration, member selection, and overcoming…

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Navigating sIRB Complexities: An Interactive Session

Got questions about sIRBs? Join experts as they share insights and priorities, plus a Q&A…

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Sponsors: Are Your Sites Ready for an FDA Inspection?

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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How Genetic Engineering Will Move Rare Disease Research at Warp Speed

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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What Happens When a Study Fails to Meet Its Recruitment Targets?

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Best Practices for IRB Review of DCTs: Expert Perspectives

A variety of distinctive ethical, regulatory, and legal challenges stand in the way of greater…

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sIRB 101: An Introduction to Relying on an External IRB

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Inspection Readiness: Before, During, After

Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and…

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Don’t Get Caught Off Guard: Inspection Readiness for Sponsors and CROs

An inspection readiness program can assess compliance, address deficiencies, and prepare sponsors and CROs for…

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