Code of Federal Regulations (Last Updated: November 8, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter C - Drugs: General |
Part 203 - Prescription Drug Marketing |
Subpart A - General Provisions |
§ 203.1 - Scope. |
§ 203.2 - Purpose. |
§ 203.3 - Definitions. |
Subpart B - Reimportation |
§ 203.10 - Restrictions on reimportation. |
§ 203.11 - Applications for reimportation to provide emergency medical care. |
§ 203.12 - An appeal from an adverse decision by the district office. |
Subpart C - Sales Restrictions |
§ 203.20 - Sales restrictions. |
§ 203.22 - Exclusions. |
§ 203.23 - Returns. |
Subpart D - Samples |
§ 203.30 - Sample distribution by mail or common carrier. |
§ 203.31 - Sample distribution by means other than mail or common carrier (direct delivery by a representative or detailer). |
§ 203.32 - Drug sample storage and handling requirements. |
§ 203.33 - Drug sample forms. |
§ 203.34 - Policies and procedures; administrative systems. |
§ 203.35 - Standing requests. |
§ 203.36 - Fulfillment houses, shipping and mailing services, comarketing agreements, and third-party recordkeeping. |
§ 203.37 - Investigation and notification requirements. |
§ 203.38 - Sample lot or control numbers; labeling of sample units. |
§ 203.39 - Donation of drug samples to charitable institutions. |
Subpart E - Wholesale Distribution |
§ 203.50 - Requirements for wholesale distribution of prescription drugs. |
Subpart F - Request and Receipt Forms, Reports, and Records |
§ 203.60 - Request and receipt forms, reports, and records. |
Subpart G - Rewards |
§ 203.70 - Application for a reward. |