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 Code of Federal Regulations (Last Updated: November 8, 2024)
 Title 21 - Food and Drugs
 Chapter I - Food and Drug Administration, Department of Health and Human Services
 SubChapter C - Drugs: General
 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
 Subpart E - Electronic Format for Registration and Listing

  Subpart E - Electronic Format for Registration and Listing  

§ 207.61 - How is registration and listing information provided to FDA?
§ 207.65 - How can a waiver of the electronic submission requirement be obtained?