DIA - Drug Information Association, Online Webinar
July 9, 2009 - July 23. 2009
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)
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