21 CFR Part 203
PART 203—PRESCRIPTION DRUG MARKETING
- PART 203—PRESCRIPTION DRUG MARKETING
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter C—Drugs: General
- 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.
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