U.S. Food and Drug Administration
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The U.S. Food and Drug Administration (FDA) is a regulatory commission that oversees food, drugs, medical devices, vaccines, tobacco products and more for the United States. To date, the FDA has not approved any drugs for the use of Myalgic Encephalomyelitis & Chronic Fatigue Syndrome (ME/CFS).
FDA activities on drug development for Myalgic Encephalomyelitis & Chronic Fatigue Syndrome[edit | edit source]
- Apr, 23, 2014 FDA Webinar: Guidance for Industry Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis: Developing Drug Products for Treatment by Janet Maynard, MD, MP
- Mar 11, 2014, Federal Register Notice of Draft Guidance for Industry on Chronic Fatigue Syndrome/Myalgic Encephalomyelitis: Developing Drug Products for Treatment; Availability
- Mar 10, 2014, Guidance for Industry Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis: Developing Drug Products for Treatment (12 pages)
- Oct 16, 2013, Chronic Fatigue Syndrome and Myalgic Encephalomyelitis (CFS and ME) Stakeholder Teleconference Transcript of Teleconference
- Apr 26, 2013, CFS and ME Meeting Summary
- Apr 25-26, 2013, FDA Workshop on Drug Development for Chronic Fatigue Syndrome (CFS) and Myalgic Encephalomyelitis (ME)
- Apr 25, 2013, "The Voice of the Patient" - Report on FDA public meeting for ME/CFS
- Apr 18, 2013, FDA 101 Webinar by David Banks. PhD
- Nov 15, 2012, Myalgic Encephalomyelitis and Chronic Fatigue Syndrome Webinar: Working Together for Change
- Sept 13, 2012, Teleconference between FDA and Patients/Patient Advocates
