Overview:
This informative session will cover these new requirements for auditing clinical trials, evaluate the changes and understand how these impact on auditors.
This will enable you to meet the new international GCP standard to ensure the acceptance of clinical trial data by the regulatory authorities internationally including the European Union (EU), Japan, the United States, Canada and Switzerland.
This informative session will cover these new requirements for auditing clinical trials, evaluate the changes and understand how these impact on auditors.
This will enable you to meet the new international GCP standard to ensure the acceptance of clinical trial data by the regulatory authorities internationally including the European Union (EU), Japan, the United States, Canada and Switzerland.
Who Should Attend
- Clinical Research Managers, VPs and Directors
- Quality Assurance for Clinical Trials /GXP
- Study Site Staff including investigators
- CROs and Other Vendors Working on Clinical Trials
- Data Management
- Pharmacovigilance for Clinical Trials
- R
