1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter F - BIOLOGICS
  5. 21 CFR Part 607
21 CFR Part 607
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
June 25, 2020
Subpart
B
Procedures for Domestic Blood Product Establishments
Subpart
A
General Provisions
Subpart
C
Procedures for Foreign Blood Product Establishments
Subpart
D
Exemptions
Subpart
E
Establishment Registration and Product Listing Of Licensed Devices
Previous
Part 606 CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
Next
Part 610 GENERAL BIOLOGICAL PRODUCTS STANDARDS

Tried the LawStack mobile app?

Join thousands and try LawStack mobile for FREE today.

  • Carry the law offline, wherever you go.
  • Download CFR, USC, rules, and state law to your mobile device.

Designed and built by Tekk Innovations LLC, the makers of the LawStack iPhone app or Android app.

© 2020 Tekk Innovations LLC