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.