FDA will host Rare Disease Day, a virtual public meeting, on March 1, 2024 in global observance of Rare Disease Week. This year’s Rare Disease Day is dedicated to patients and health care professionals. Panels will discuss:
- The legal framework for approving studies and medical products at FDA
- What FDA does during review processes to approve medical products
- Decentralized clinical trials and digital health technologies
- Where to find important information and documents related to clinical trials
- Information that can be obtained from medical product labels
- Legal and ethical requirements for consent forms in clinical trials
- FDA initiatives to advance medical product development for rare diseases
- Ways for patients to engage with FDA