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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 F - BIOLOGICS
  6. PART 606 - CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS

21 CFR Part 606 - CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS

  • CFR
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  1. Subpart A - General Provisions (§ 606.3)
  2. Subpart B - Organization and Personnel (§ 606.20)
  3. Subpart C - Plant and Facilities (§ 606.40)
  4. Subpart D - Equipment (§§ 606.60 - 606.65)
  5. Subpart E [Reserved]
  6. Subpart F - Production and Process Controls (§§ 606.100 - 606.110)
  7. Subpart G - Additional Labeling Standards for Blood and Blood Components (§§ 606.120 - 606.122)
  8. Subpart H - Laboratory Controls (§§ 606.140 - 606.151)
  9. Subpart I - Records and Reports (§§ 606.160 - 606.171)
Authority:
21 U.S.C. 321, 331, 351, 352, 355, 360, 360j, 371, 374; 42 U.S.C. 216, 262, 263a, 264.
Source:
40 FR 53532, Nov. 18, 1975, unless otherwise noted.

The following state regulations pages link to this page.



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