FDA-PATIENT-PREFER › Complete Document History
Patient Preference Information - Voluntary Submission, Review in Premarket Approval Applications, Humanitarian Device Exemption Applications, and De Novo Requests, and Inclusion in Decision Summaries and Device Labeling - Guidance for Industry, Food and Drug Administration Staff, and Other Stakeholders
Complete Current Edition: |
2016 EDITION - Guidance for Industry, Food and Drug Administration Staff, a - Aug. 24, 2016
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Obsolete Revision Information: |
2015 DRAFT - Draft Guidance for Industry, Food and Drug Administration St - May 14, 2015
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