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WCG Webinar Series – Join us for three upcoming webinars addressing clinical trial safety reporting, site identification and feasibility, and site activation:
Optimizing Global Safety Reporting in Clinical Trials
Eliminating Overdistribution of Safety Reports, Reducing Site Burden, Increasing Patient Safety
Global safety reporting has become increasingly difficult for sponsors and sites to manage. Fearing regulatory repercussions, sponsors inundate investigative sites with numerous non-actionable reports. Investigators are forced to endure this barrage, but at the expense of patient safety. How do we break this inefficient—and ineffective—cycle?
Join industry experts Kendra Hayden of Hoffman-la Roche Limited, along with Steven Beales and Kristy Fusco of ePharmaSolutions, as they explain how leveraging global expertise and using the proper technology can improve the safety reporting process.
 Date: Monday, October 30th
 Time: 10:00 AM ET | 2:00 PM GMT
Complimentary webinar. Space is limited. Register today. |
Speed, Efficiency and Accuracy in
Site Contracts and Payments
Five Essential Considerations for Trial Sponsors
For most sponsors, the negotiation and execution of site contracts, investigator budgets, and site payments can be challenging. Often managed independently, these three services are deeply interrelated, and any lack of coordination between them results in added cost and significant delay.
Join Clintrax Global for a one-hour webinar during which Russell John, Clintrax’s Vice President of Grants Management, will present the five essential considerations for driving speed, efficiency and accuracy in the coordination and negotiation of investigator contracts, budgets and payments.
Date: Monday, November 6th
Time: 10:00 AM EST | 3:00 PM GMT
Complimentary webinar. Space is limited. Register today. |
Solving the Problem of Clinical Research Enrollment
Conditions that Affect Enrollment and Strategies to Increase It
Our industry has literally spent billions of dollars trying to solve the problem of low and non-enrollment in clinical trials. Nonetheless, we continue to see an average non-enrollment rate of 20% across the industry. Why is this problem so challenging? And why haven’t we made more substantial progress toward solving it?
Join industry expert Suzanne Caruso, Vice President of Clinical Solutions for the WIRB-Copernicus Group, for a one-hour webinar during which she will examine the conditions that affect enrollment, and offer strategies to ultimately increase it.
Date: Monday, November 13th
Time: 10:00 AM EST | 3:00 PM GMT
Complimentary webinar. Space is limited. Register today. |
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