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Part 203
FEDERAL · 21 CFR
Part 203 — Prescription Drug Marketing
22 sections · Title 21: Food and Drugs
§ 203.1
Scope.
§ 203.2
Purpose.
§ 203.3
Definitions.
§ 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.
§ 203.20
Sales restrictions.
§ 203.22
Exclusions.
§ 203.23
Returns.
§ 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.
§ 203.50
Requirements for wholesale distribution of prescription drugs.
§ 203.60
Request and receipt forms, reports, and records.
§ 203.70
Application for a reward.