This GCP training Webinar will discuss the principals of GCP, the regulations pertaining to it and elements necessary for FDA compliance.
Areas Covered in the Seminar:
- Discuss the FDA s role in Drug Development.
- Principles of GCP.
- Activities that are common to most trials.
- Summarize FDA GCP regulations.
- Recognize how GCP impacts the clinical research process.
- Prepare concise documents and provide.
- Necessary information for clinical studies compliance.
- Maintain ongoing compliance.
Who Will Benefit:
This webinar will provide valuable assistance to all personnel in: Pharmaceutical, Biotechnology, CROs and Research Facilities Conducting Clinical Trials including:
- Managers in Clinical Development and Project Leaders
- Quality Assurance Managers and auditors
- Clinical Research Associates
- Clinical Operations Staff
- Regulatory Compliance Associates and Managers
