CenterWatch Announces — Final ICH E6 (R2) Guideline on Good Clinical Practices: The Real Impact of the Changes Webinar May 27, 2020

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How will the updated ICH E6 (R2) affect clinical trial strategies? This webinar explains the impact of the changes.

WCG CenterWatch

WCG CenterWatch

Final ICH E6 (R2) Guideline on Good Clinical Practices
The Real Impact of the Changes
A CenterWatch Webinar
Wednesday, May 27, 2020, 1:30-3:00 p.m. EDT

What impact will the revisions to ICH E6 (R2) have on clinical trials and organizational practices? Find out during our comprehensive webinar.

The Integrated Addendum to ICH E6 (R1): Guideline for Good Clinical Practice E6 (R2) (GCP E6 R2) contains 26 significant changes, such as: new sections on investigator responsibilities, a new sponsor section on quality management, new section on computer validation and electronic records as well as updates on monitoring plans, risk-based quality management system and serious breaches.

In this upcoming webinar, Marina Malikova, Ph.D., MSci, MA, CCRA, RAC, will discuss changes impacting the roles and responsibilities of investigators, sites, sponsors and CROs. She will share best practices for resource allocation and adjustments for organizations:

●GCP E6 Guideline R2 Addendum overview and areas of changes, including new sections on investigator responsibilities and the substantial new sponsor section on quality management
●Implementation of revised regulatory guidelines, including those affecting globalization issues
●Introduction of risk-based quality management (RBQM), including those affecting serious breaches
●Development of SOPs, including those on validation and electronic records

Be ready to implement new approaches to clinical trial design, conduct, oversight, recording and reporting?

Interested in registering multiple sites?
Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally to learn about our special multisite discount.

Webinar Details:
Final ICH E6 (R2) Guideline on Good Clinical Practices
The Real Impact of the Changes
A CenterWatch Webinar
Wednesday, May 27, 2020, 1:30-3:00 p.m. EDT

$287 per site

Easy Ways to Register:
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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Michelle Butler
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