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Clinical Trials in the Era of Precision Medicine
Webinar: Addressing Acceptable Recruitment Methods for Sponsors & Sites
Webinar: Gene Therapy for Rare and Ultra-rare Diseases
Rare & Orphan Disease Endpoints: Challenges & Examples from Neurodevelopment
Recruiting Patients & Time Management: Top Tips for Dealing with the Most Critical Resource in Research
Learn how to engage sites more effectively with the appropriate recruitment resources, use dedicated staff to manage recruitment efforts, and eliminate bottlenecks and expedite recruitment timelines.
Harnessing the Power of Data to Optimize Site Selection for Clinical Trials
In this webinar, we explore the untapped value of your own internal study data, all the available open-data sources, and the amazing potential of IRB data in achieving full clinical trial enrollment.
Strategies that Inform Investigator Selection and Enhance Enrollment
Learn how to use predictive analytics and strategic consulting to guide site selection and enrollment success.
Understanding the Challenges of Managing Combination Product Safety Reporting
Do the Right Thing: Unique Ethical Issues in Oncology Research
Placebo Response in Clinical Trials: Approaches to Mitigation
Industry trends show that a major contributor to trial failure is the increased rate of placebo response.Watch this webinar to learn how to increase the chances of trial success in an uncertain world.
Operationalizing the NIH Single IRB Mandate
The National Institutes of Health’s (NIH) new policy mandating the use of a single Institutional Review Board (sIRB) for all multi-site studies goes into effect in September 2017. Are you ready?
Optimizing Global Safety Reporting in Clinical Trials
Learn how a large, global pharmaceutical company saved millions of dollars by optimizing their safety reporting process.
Solving The Problem of Clinical Research Enrollment
Examine the conditions that affect enrollment and learn strategies to increase it.
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
In June of 1966, physician-researcher Henry K. Beecher published a paper entitled “Ethics and Clinical Research.” Explore the history and motivation that led to Dr. Beecher’s ground-breaking paper.
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