Part I
Index
- Introduction
- Federal Oversight over Drugs and an Overview of the Food and Drugs Act
- Market Authorization of Drugs Under the Food and Drug Regulations
- Prescription Drugs
- Establishment Licensing and Good Manufacturing Practices for Drugs
- On-Market Rules and Authorities
- Other Ways in Which a Drug May Be Sold: Clinical Trials, Special Access, Extraordinary Use, Urgent Public Health Need, and Shortages
- Other Classes of Drugs - Biologics, Blood, 'Cells, Tissues, and Organs,' and Radiopharmaceuticals
- Natural Health Products
- Veterinary Drugs
- COVID-19 Interim Orders