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 |
Description
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