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Patient Voices Report.pdf

UCM368806.pdf
Preview of Patient Voices Report
🔗 Source: fda.gov
📊 Size: 267 KB
👤 Author: fda/cder
⬇️ Downloads: 64

Summary

The FDA held a public meeting on April 25, 2013, to hear from patients with Chronic Fatigue Syndrome (CFS) and Myalgic Encephalomyelitis (ME) about their disease, its impact on daily life, and available therapies. The meeting focused on two topics: disease symptoms and daily impacts, and patient perspectives on treating CFS and ME. Patients and patient representatives shared comments, and a facilitated discussion invited additional comments from the audience. The meeting was part of the FDA's Patient-Focused Drug Development initiative, which aims to gather patient perspectives on their condition and available therapies. A separate report summarizes comments submitted to a public docket, which was open until August 2, 2013. The report reflects patient perspectives on disease symptoms, impacts, and current treatments, but is not representative of any specific group's views or experiences.

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Description

The FDA held a public meeting on April 25, 2013, to hear from patients with Chronic Fatigue Syndrome (CFS) and Myalgic Encephalomyelitis (ME) about their...

Technical Information

  • File Format: PDF
  • File Size: 267 KB
  • Pages: 23
  • Language: EN
  • Author: fda/cder
  • Total Downloads: 64
  • Last Updated: 1 week ago

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体育会ナビの説明会は親しみやすく楽しいと参加学生から評価され、質疑応答の時間も設けられてとても有意義だった。企業理念や勤務条件についても現場の声を聞くことができた。
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