The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
05 Oct 2010
Webinar
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
Past Events
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development - 05 Oct 2010, Webinar (8654)
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development 2026
Important
Please, check "The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development" official website for possible changes, before making any traveling arrangements
