21 CFR Part 607 - ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
- Subpart A—General Provisions (§§ 607.1 - 607.7)
- Subpart B—Procedures for Domestic Blood Product Establishments (§§ 607.20 - 607.39)
- Subpart C—Procedures for Foreign Blood Product Establishments (§ 607.40)
- Subpart D—Exemptions (§ 607.65)
- Subpart E—Establishment Registration and Product Listing Of Licensed Devices (§ 607.80)