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United States Code (Last Updated: May 24, 2014) |
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Title 21. FOOD AND DRUGS |
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Chapter 9. FEDERAL FOOD, DRUG, AND COSMETIC ACT |
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SubChapter V. DRUGS AND DEVICES |
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Part E. General Provisions Relating to Drugs and Devices |
| § 360bbb. Expanded access to unapproved therapies and diagnostics |
| § 360bbb–1. Dispute resolution |
| § 360bbb–2. Classification of products |
| § 360bbb–3. Authorization for medical products for use in emergencies |
| § 360bbb–3a. Emergency use of medical products |
| § 360bbb–3b. Products held for emergency use |
| § 360bbb–4. Countermeasure development, review, and technical assistance |
| § 360bbb–5. Critical Path Public-Private Partnerships |
| § 360bbb–6. Risk communication |
| § 360bbb–7. Notification |
| § 360bbb–8. Consultation with external experts on rare diseases, targeted therapies, and genetic targeting of treatments |
| § 360bbb–8a. Optimizing global clinical trials |
| § 360bbb–8b. Use of clinical investigation data from outside the United States |
| § 360bbb–8c. Patient participation in medical product discussion |