FALLS CHURCH, Va., March 20, 2019 /PRNewswire-PRWeb/ -- ICH GCP E6 R2 Meeting CRO-Vendor Oversight Requirements **An
ICH GCP E6 R2: Meeting CRO-Vendor Oversight Requirements starts in one week. For clinical trials, it's a whole new game.
The ICH GCP E6 R2 guidelines now require sponsors/CROs to implement a CRO-vendor oversight framework… procedures… methods… oversight plans… and equipping staff to ensure compliance, meet regulatory expectations and maintain a constant state of control over the trial, CRO-vendors and inspection readiness.
Whether the organization is virtual, small, medium or large, the requirements are the same.
FDAnews has teamed up with Wool Consulting Group to present a two-day hands-on workshop aimed at helping one understand and comply with new ICH GCP E6 R2 rules. Course instructor — Liz Wool, CCRA, CID, CMT — will provide methods and solutions for effective implementation of the rules. Over the course of two days she'll:
Through presentations, discussion, class activities and handouts attendees will learn how to implement ICH GCP E6 R2 requirements in the organization.
Reminder: ICH GCP E6 R2: Meeting CRO-Vendor Oversight Requirements starts in one week.
Meet Your Presenter: Liz Wool, CCRA, CID, CMT has 29 years clinical research experience in clinical operations, compliance, CRO-vendor oversight and training, She is a certified CRA (ACRP), instructional designer and master trainer and a member of the National Speakers Association. She is a recognized industry expert on CRO-vendor oversight/management who has presented on this topic in both the United States and the European Union since 2010 for both nonprofit professional associations (DIA) and industry conferences.
Who Will Benefit:
Webinar Details: ICH GCP E6 R2 Meeting CRO-Vendor Oversight Requirements **An interactive workshop presented by CenterWatch and Wool Consulting Group** March 27-28, 2019 Raleigh, NC http://store.centerwatch.com/p-581-ich-gcp-e6-r2-meeting-cro-vendor-oversight-requirements.aspx
Tuition: Regular Pricing: $1,797 (after Mar. 1, 2019) Significant team discounts are available.
Easy Ways to Register: Online: http://store.centerwatch.com/p-581-ich-gcp-e6-r2-meeting-cro-vendor-oversight-requirements.aspx By phone: 888-838-5578 or 703-538-7600
About CenterWatch: Founded in 1994, CenterWatch is a trusted source and global destination for clinical trials information for both professionals and patients. CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, CROs, SMOs, and investigative sites involved in the management and conduct of clinical trials. As a pioneer in publishing clinical trials information, CenterWatch was the first Internet site to publish detailed information about active clinical trials that could be accessed by patients and their advocates.
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