The Importance of the Investigator Responsibilities and Legal Commitments in Drug and Device Clinical Research in Achieving a Clean Audit 2016 is a webinar that covers topics such as:
- How following GCP helps assure a clean Audit / inspection?
- The Investigators key role in the clinical research process
- What are the main Investigator responsibilities?
- The difference between AEs and SAEs and the reporting requirements
- What is the legal language of the FDA form 1572 or Device equivalent?
- How is the investigator responsible for the IC process?
- Why is Financial Disclosure information important?
The Importance of the Investigator Responsibilities and Legal Commitments in Drug and Device Clinical Research in Achieving a Clean Audit 2016 is intended for attendees from:
- Clinical Research Scientists (PKs, Biostatisticians)
- Principal Investigators and Sub Investigators
- Clinical Research Associates (CRAs) and Coordinators (CRCs)
- Safety Nurses
- QA / QC Auditors and Staff
- Recruiting Staff
- Clinical Research Data Managers
