Regulation Text
Authority
21 U.S.C. 321,331,351,352,353,355,360bbb,371;42 U.S.C. 262.
Related Warning Letters (1)
- 2022-02-22
New Drug/Labeling/Misbranded
CytoDyn, Inc.
Related Guidelines (6)
IND Exemptions for Studies of Lawfully Marketed Drug or Biological Products for the Treatment of Cancer: Guidance for Industry (Status: Final)
→Informed Consent: Guidance for IRBs, Clinical Investigators, and Sponsors (Status: Final)
→Recruiting Study Subjects: Guidance for Institutional Review Boards and Clinical Investigators (Status: Final)
→Exception from Informed Consent Requirements for Emergency Research: Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors (Status: Final)
→Expanded Access to Investigational Drugs for Treatment Use: Questions and Answers (Status: Final)
→Drug and Device Manufacturer Communications With Payors, Formulary Committees, and Similar Entities – Questions and Answers: Guidance for Industry and Review Staff (Status: Final)
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