Clinical Trial Monitoring - Documentation and Closure 2016 is a webinar that covers topics such as:
- Case Report Forms vs Source Documents: Can these be kept electronically?
- Essential documents: What are they? Where can I get examples? Who is responsible for maintaining and generating these?
- Sample materials such as a study closure checklist
- Considerations when deciding to close a study
- Common audit findings and how to avoid these
- Close out visit and Internal audits practices
- ICH GCP E6
Clinical Trial Monitoring - Documentation and Closure 2016 is intended for:
- Healthcare interested in exploring the field of Clinical Research
- Human Subjects Research
- Administration in charge of Clinical Research, Clinical Research Sites
- Clinical Research Coordinator positions
- Principal Investigator positions, Sub-Investigators
- Contract Research Organizations , Clinical Research Associates, Regulatory Coordinators
- Monitors and auditors
