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U.S. Food & Drug Administration
Continuing Education and Accreditation
Division of Learning and Organizational Development
Center for Drug Evaluation and Research

FDA Rare Disease Day 2024: Navigating Information. Empowering Patients and Providers

Enroll
Step Status
Educational Content ✘
Posttest ✘
Evaluation ✘
Starts On: Mon, 4/29/24: 12:00 AM EDT
Ends On: Wed, 4/28/27: 12:00 AM EDT
Type: Enduring Material
Credits: 2
Description: In this enduring material, FDA experts discuss how to find information related to FDA-approved drugs, information on clinical trials, and how to understand informed consent documents for clinical trials.
Objectives:
  • Identify where to find important information and documents related to clinical trials and medical products in the United States.
  • Define the types of information that can be obtained from medical product labels.
  • Explain, in general terms, the legal and ethical requirements for consent forms in clinical trials.
Additional Information: Review the Activity Announcement for additional details: Announcement Form