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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER C—DRUGS: GENERAL
  6. PART 207—REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTABLISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, INCLUDING DRUGS THAT ARE REGULATED UNDER A BIOLOGICS LICENSE APPLICATION, AND ANIMAL DRUGS, AND THE NATIONAL DRUG CODE
  7. Subpart B—Registration

21 CFR Part 207 - Subpart B - Registration

  • CFR
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  1. § 207.17 Who must register?
  2. § 207.21 When must initial registration information be provided?
  3. § 207.25 What information is required for registration?
  4. § 207.29 What are the requirements for reviewing and updating registration information?

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