Good Clinical Practices for the Clinical Research Professional - 4 Part On-line Training Series (Par

Venue: Online Webinar

Location: Horsham, Pennsylvania, United States

Event Date/Time: Jul 09, 2009
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Description

Part 1 of 4 Part On-line Training Series

Overview
Gain the knowledge required to conduct clinical trials, including knowledge about subject safety, regulations, and the practicalities of performing research studies.

What You Will Learn
  • Roles and responsibilities of each member of the study team
  • Regulations and guidelines that govern clinical investigations
  • Consent elements and consent process
  • Successful patient recruitment and retention strategies
  • Importance of study compliance during clinical trials
  • Preparing for audits and audit process


Target Audience
  • Clinical investigators
  • Clinical research professionals
  • Sub-investigators


  • Study staff




Part 1: Roles and Responsibilities – Thursday, July 9, 2009 (12:00-2:00 pm)

Part 2: Regulations and Guidelines that Govern Clinical Investigation - Thursday, July 16, 2009 (12:00-2:00 pm)

Part 3: Practices that Ensure Effective and Efficient Study Conduct - Wednesday, July 22, 2009 (12:00-2:00 pm)

Part 4: Practices that Ensure Effective and Efficient Study Conduct (Cont’d) - Thursday, July 23, 2009 (12:00-

2:00 pm)

Speakers Include
  • Bernadette Ott
    Consultant, Good Clinical Practices/Quality Assurance
    United States




Event Code:
09487

More information: Please Click Here

Contact Information
For detailed program information including faculty and topics, please contact:

Colleen Buckley
Tel. 215-442-6108
Email Colleen.Buckley@diahome.org

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