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WCG Announces — Safety Reporting in Global Clinical Trials: Maximizing Compliance, Minimizing Costs, Free Webinar, Sept. 27, 2018

Safety Reporting in Global Clinical Trials:
Maximizing Compliance, Minimizing Costs
**WCG Free Webinar**
Sept. 27, 2018 — 1:30 p.m. – 3:00 p.m. ET

Clinical research organizations (CROs) may be spending too much on safety reporting by as much as fifty percent.

This can be due to a lack of automated systems to distribute the right safety information to the right investigators and ECs at the right time using local Country Alerting rules.

The largest trial sites may receive up to 50 safety reports per day and spend an average of two hours processing them. That adds up.

When trial sponsors compensate by over-distributing safety reports, it merely increases costs. It can also introduce compliance and tracking issues, and steal investigator time from patients.

Mark the calendar for Thursday, Sept. 27, for a free webinar from WCG/CenterWatch, where attendees will discover a new approach to this costly problem.

Steven Beales, senior VP-IT and Market Owner of Safety Solutions at ePharmaSolutions, is an expert in the field of safety reporting technology. At ePharmaSolutions, he has implemented the company’s Clinical Trial Portal at Genentech across more than 100 countries.

He is joined by Kendra Hayden, Global Process Owner, Safety Document Distribution, Roche. Her focus is process management within clinical operations in global safety document distribution for investigators and ethics committees. Together, they will introduce attendees to new efficiencies in safety reporting and demonstrate ways to:

  •     Cut safety reporting costs by > 50%
  •     Reduce site burden by 10 hours per week
  •     Understand global safety reporting regulations
  •     Discover how to maximize control over global safety reporting
  •     And much more

There’s little point spending money needlessly. Discover a new approach to an old problem with this presentation.

Meet the Presenters:
Steven Beales, SVP IT and Market Owner, Safety Solutions, ePharmaSolutions
Steven Beales is an expert in the field of safety reporting technology, Steven has 25 years of experience in IT, and has spent more than 16 years in the pharmaceutical industry. He joined ePharmaSolutions in in 2009 and led implementation of the company’s Clinical Trial Portal at Genentech across more than 100 countries.

Kendra Hayden, Global Process Owner, Safety Document Distribution, Roche
Kendra Hayden has been at Roche for 20+ years. During that time, she has held many roles such as a monitor, compliance and training, and process management. Her current area of focus is process management within clinical operations, specifically in the area of Global Safety Document Distribution for Investigators and Ethics Committees. Within this focus, she serves as the global process owner and project business lead.

Who Will Benefit:
This presentation is aimed at pharma and biotech CROs:

  •     Medical director
  •     Clinical safety executive
  •     Study coordinator responsible for subject recruitment

Webinar Details:
Safety Reporting in Global Clinical Trials:
Maximizing Compliance, Minimizing Costs
**WCG Free Webinar**
Sept. 27, 2018 — 1:30 p.m. – 3:00 p.m. ET

Easy Ways to Register:
By phone: 888-838-5578 or 703-538-7600

WIRB-Copernicus Group® (WCG):
The pioneer of independent ethical review, WCG continues to drive ingenuity in the clinical research space. Today, WCG’s solutions are built upon the foundation of ethical review, but have grown to include a suite of complementary services and technologies that expand the capabilities of the modern research professional. WCG delivers transformational solutions that stimulate growth, foster compliance, and maximize efficiency for those who perform clinical trials.

Read the full story at

Source: PRWeb
Copyright©2018 Vocus, Inc.
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