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Addressing Acceptable Recruitment Methods
Gene Therapy for Rare and Ultra-rare Diseases
Rare & Orphan Disease Endpoints: Challenges & Examples from Neurodevelopment
Strategies that Inform Investigator Selection and Enhance Enrollment
Understanding the Challenges of Managing Combination Product Safety Reporting
Bigger, Better, Faster and More: How Institutions Can Increase Funding, Improve Research and Speed Enrollment
Do the Right Thing: Unique Ethical Issues in Oncology Research
Placebo Response in Clinical Trials: Approaches to Mitigation
Operationalizing the NIH Single IRB Mandate
Optimizing Global Safety Reporting in Clinical Trials
Solving The Problem of Clinical Research Enrollment
Speed, Efficiency and Accuracy in Site Contracts and Payments
Learn how sponsors and CROs can optimize site contracting and payments management to expedite the process of contract negotiation, reducing both the cycle time and burden on the legal infrastructure.
Fifty Years of Change: Henry K. Beecher and Protecting Human Subjects
Harnessing the Power of Data to Optimize Site Selection for Clinical Trials
A Discussion of the Revised Common Rule - Jan 2017
Early Access to Investigational Drugs: Lessons Learned from Ebola
Learn about the regulatory framework that governs the use of investigational drugs outside clinical trials (formerly called “compassionate use”), and the ethical challenges surrounding it.
Clinical Data Disclosure: The Complicated Efforts to Make Research Transparent
Learn status of the requirements and recommendations for data-sharing from EMEA, FDA and PhRMA, and how to determine the steps to navigate the complicated field of data transparency compliance.
IRBNet and VA Medical Centers: A Powerful Partnership Made Even Easier