Safety Management > QUESTIONS & ANSWERS > Investigator-Initiated Studies / FDA & GCP Compliance Guide / 2025 Update / Score 100% (All)

Investigator-Initiated Studies / FDA & GCP Compliance Guide / 2025 Update / Score 100%

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Master the protocols for Conducting Investigator-Initiated Studies (IIS) according to FDA regulations and Good Clinical Practice (GCP) with our 2025 updated guide. This essential resource is designed ... for principal investigators, clinical researchers, and study coordinators preparing for certification exams or real-world trial management. It covers critical topics including IND applications, IRB collaboration, informed consent, safety reporting, and monitoring responsibilities. With detailed explanations and a targeted test bank, you can ensure regulatory compliance, pass your certification, and score 100% on FDA and GCP assessments. [Show More]

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