DrugDev and SCRS Present Educational Webinar on How to Develop an Efficient and Compliant Clinical Trial Start-Up Process

The new educational webinar will will demonstrate how Good Clinical Practice (GCP) can be used throughout the clinical trial site activation process with an emphasis on feasibility, contracts, and site documents.

DrugDev and the Society for Clinical Research Sites (SCRS) will host a new educational webinar to demonstrate how Good Clinical Practice (GCP) can be used throughout the site activation process with an emphasis on feasibility, contracts, and site documents. In addition the webinar will discuss the importance of GCP compliance, how sites are affected by GCP during selection and activation, and common site mistakes that can be avoided.

In 1997 the FDA ratified 13 laws for establishing GCP during clinical trials, endorsing ethics practices that had been evolving since the Nuremberg Code in 1947. As a result GCP has been the standard guide for conducting clinical trials for sponsors, sites, and investigators ever since.

SCRS Webinar: How to Develop an Efficient and Compliant Start-Up Process

Webinar Date: August 15, 2017

Time: 12:00-1:00 PM ET

Presenters: Chibuzor Ebhogiaye, SiteStart Lead, DrugDev; Angel Mann, Product Support Specialist, DrugDev

Registration: Register Here

(Free for SCRS members, $79.00 for non-members)

At the conclusion of the webinar attendees will be able to:

  • Understand how sites are affected by GCP
  • Identify how organizations can manage GCP during the activation process
  • Learn common site mistakes and how to overcome them
  • Understand the importance of GCP compliance during site activation

About the Presenters

Chibuzor Ebhogiaye is a lead with the SiteStart team in DrugDev’s London office. She is focused on site identification, site management and contract management services. She developed a love for clinical trials during an internship at Roche and has worked in the industry ever since. Chibuzor is passionate about building relationships and sharing best practices between sites and sponsors to create a smoother trial process.

Angel Mann has a thorough knowledge and understanding of clinical trials and study startup. She is experienced in building a strong foundation for an efficient trial by communicating with sponsors and sites about their specific needs, and…

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