21 C.F.R. PART 207--REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION
TITLE 21--Food and Drugs
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER C--DRUGS: GENERAL
PART 207--REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION
Subpart A--GENERAL
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| Establishment registration and product listing for human blood and blood products and for medical devices.
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Subpart B--EXEMPTIONS
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| Exemptions for establishments.
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Subpart C--PROCEDURES FOR DOMESTIC DRUG ESTABLISHMENTS
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| Who must register and submit a drug list.
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| Times for registration and drug listing.
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| How and where to register and list drugs.
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| Information required in registration and drug listing.
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| Amendments to registration.
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| Updating drug listing information.
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| Additional drug listing information.
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| Notification of registrant; drug establishment registration number and drug listing number.
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| Inspection of registrations and drug listings.
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| Misbranding by reference to registration or to registration number.
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Subpart D--PROCEDURE FOR FOREIGN DRUG ESTABLISHMENTS
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| Establishment registration and drug listing requirements for foreign establishments.
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