CenterWatch Announces — ICH E8 Developments: Are You Sure You’re Up to Date? Webinar, Nov. 19, 2019

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Conducting clinical trials? ICH E8(R1) impacts each trial. What MUST change in current SOPs, procedures, processes and documentation.



Are You Sure You’re Up to Date?
**A CenterWatch Webinar**
Tuesday, Nov. 19, 2019, 1:30-3:00 p.m. EDT

Are the current clinical studies of one’s organization ready to incorporate achieving fit-for-purpose data quality?

With ICH E8(R1) set to be adopted in June 2020, planning, design and conduct of clinical trials will look different than they do today. Make sure to be ready to implement the new guidelines.

Leslie Sam — Principal Consultant with Wool Consulting Group and over 20 years’ experience as a clinical research and quality professional — will share how to leverage the revised guidelines’ quality-by-design approaches, expanded study designs and data source considerations. With this knowledge, attendees can adapt, continuing to provide a quality-driven framework that leads to efficient and timely decision making, and ultimately to improved access to safe and effective drugs.

In this webinar, Ms. Sam will:

  • Explain the scope and general principles of the ICH E8(R1) guideline
  • Describe the impact to current research practices that may be outlined in SOPs, procedures, processes and documentation
  • Describe the framework and approaches for identifying critical to quality factors
  • Identify clinical development areas that may be impacted by the adoption of the ICH E8(R1) guideline and approaches for compliance

Prepare for ICH E8(R1) now, or risk being left behind.

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:
ICH E8 Developments
Are You Sure You’re Up to Date?
**A CenterWatch Webinar**
Tuesday, Nov. 19, 2019, 1:30-3:00 p.m. EDT

Easy Ways to Register:
By phone: 617-948-5100 or 866-219-3440

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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