Title 21--Food and Drugs

CHAPTER I--FOOD AND DRUG ADMINISTRATION,
DEPARTMENT OF HEALTH AND
HUMAN SERVICES

PART 207--REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION

TEXT PDF207.3 Definitions.
TEXT PDF207.7 Establishment registration and product listing for human blood and blood products and for medical devices.
TEXT PDF207.10 Exemptions for domestic establishments.
TEXT PDF207.20 Who must register and submit a drug list.
TEXT PDF207.21 Times for registration and drug listing.
TEXT PDF207.22 How and where to register and list drugs.
TEXT PDF207.25 Information required in registration and drug listing.
TEXT PDF207.26 Amendments to registration.
TEXT PDF207.30 Updating drug listing information.
TEXT PDF207.31 Additional drug listing information.
TEXT PDF207.35 Notification of registrant; drug establishment registration number and drug listing number.
TEXT PDF207.37 Inspection of registrations and drug listings.
TEXT PDF207.39 Misbranding by reference to registration or to registration number.
TEXT PDF207.40 Drug listing requirements for foreign drug establishments.

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