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World of Compliance Module

Sponsor Responsibilities

A sponsor of clinical research should:

  • Select qualified investigators
  • Provide information needed to conduct a proper investigation
  • Ensure the investigation is conducted in accordance with protocol
  • Maintain an effective IND
  • Ensure that FDA and clinical investigators are promptly informed of significant new adverse events
Qualified investigator
Lesson status: Incomplete (0% done)
Topic: page 1 of 1 (Lesson: page 11 of 30)