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 610
21 CFR Part 610
GENERAL BIOLOGICAL PRODUCTS STANDARDS
June 25, 2020
Subpart
A
Release Requirements
Subpart
B
General Provisions
Subpart
C
[Reserved]
Subpart
D
Mycoplasma
Subpart
E
Testing Requirements for Relevant Transfusion-Transmitted Infections
Subpart
F
Dating Period Limitations
Subpart
G
Labeling Standards
Previous
Part 607 ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
Next
Part 630 REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE

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