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