Description
This presentation will navigate the December 2010 Draft Guidance For Industry: "eSource Documentation in Clinical Investigations" and share with participants important information that they should know and how this might significantly affect their day to day job both as site, monitoring and data personnel if it should become final.
- Explore the new draft guidance and its impact on clinical research.
- Discuss how this draft guidance could affect current practice and the additional measures that would need to be put in place to address its recommendations.
- Apply new techniques and best practices that can be gleaned from this draft guidance in your day-to-day job.
Speaker(s):
