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Electronic Code of Federal Regulations

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e-CFR Data is current as of April 22, 2014

TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER C—DRUGS: GENERAL

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

rule

Subpart A—GENERAL

§207.3
Definitions.
§207.7
Establishment registration and product listing for human blood and blood products and for medical devices.
rule

Subpart B—EXEMPTIONS

§207.10
Exemptions for establishments.
rule

Subpart C—PROCEDURES FOR DOMESTIC DRUG ESTABLISHMENTS

§207.20
Who must register and submit a drug list.
§207.21
Times for registration and drug listing.
§207.22
How and where to register and list drugs.
§207.25
Information required in registration and drug listing.
§207.26
Amendments to registration.
§207.30
Updating drug listing information.
§207.31
Additional drug listing information.
§207.35
Notification of registrant; drug establishment registration number and drug listing number.
§207.37
Inspection of registrations and drug listings.
§207.39
Misbranding by reference to registration or to registration number.
rule

Subpart D—PROCEDURE FOR FOREIGN DRUG ESTABLISHMENTS

§207.40
Establishment registration and drug listing requirements for foreign establishments.


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