Clinical Document World

At Clinical Document World, our goal is to help you master your clinical documentation skills and strategies. Documentation is involved in just about every aspect of a clinical trial, which is why we strive to give equal focus to key steps of the process - inspection readiness, clinical quality, GCP, and the trial master file.

Learn best practices from industry leaders working at top pharmaceutical companies and contract research organizations. Incorporate new strategies and takeaways from each session into your clinical documentation process, allowing you to improve and maximize the efficiency of your clinical trial. Join us at Clinical Document World this November 2-5, 2021 for a day dedicated to inspection readiness training, followed by 3 full days of educational sessions focused on:

- Document Filing and Improvements
- Trial Master File
- Risk-Based Monitoring
- Inspection Readiness
- Clinical Metrics
- Site - Sponsor - CRO Partnerships
- Clinical Quality
- Documentation Advancements
- Quality by Design
- And many more

Others Details

Speakers: Barbara Novak, Jennifer Wilson, Gordon D. Bedford, Aryn Knight, Sally Ton, Shannon Simpson Time: 08:30 - 15:30