Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations 2018 is a webinar that covers topics such as:
- Overview of recent changes in regulatory framework
- FDA Regulations
- FDA guidance on electronic source documentation
- GCP R2 Guidelines
- Quality Management of Data
- FDA BIMO Program
- Enhancing Excellence in conduct of Clinical Trials
Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations 2018 is intended for:
- Clinical Research Associates (CRAs)
- Research Managers
- Compliance Officers
- Clinical Research Coordinators
