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Event NameRho 2017 [Webinar] What to Do with Suspected Compliance Issues at a Clinical Study Site
Event Date(s) Thursday, April 26, 2018  to Wednesday, April 26, 2017
Event Location Online, 1 p.m. ET/ 10 a.m. PT, Duration: one hour
Description Rho, a full-service contract research organization (CRO), is offering a webinar to help quality, project management, clinical and site personnel manage conflicts as well as a review of the applicable regulations and reporting requirements.

While there are a few cases of clear cut right and wrong in compliance, in many cases it is a matter of competing priorities and different perspectives. Conflicting perspectives between sites, CROs, and sponsors are common in clinical trials. The stakes are high when the quality and integrity of the data are in question.

During the webinar, experts Diane Tilley, MSN, JD, quality assurance service leader at Rho and Kristen Snipes, project director at Rho, will discuss two case studies. The first is a sponsor who voices concern over GCP and protocol compliance at a site and a CRO and the second is an investigator who raises concerns about the actions of a study coordinator at a critical point in development.
SponsorRebound Therapeutics
Host CompanyRho
Contact Information Phone: 919-408-8000
Fax:   919-408-0999 
Email: N/A
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