The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development

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.

For More Details:
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