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A UL course

Participants will be taught the general requirements of good clinical practices (GCPs) and the protection of human subjects. The course also covers the concepts, individuals, and groups involved with the GCPs process.

Featured topics

  • Regulatory authority approval for clinical trials
  • GCP requirements and international regulations
  • Five key GCP documents

Who should attend?

Professionals and experts in the pharmaceutical, biotechnology, and medical device fields

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