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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 640 - PART 640—ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
Subpart A [§ 640.1 - § 640.6] - Subpart A—Whole Blood
Subpart B [§ 640.10 - § 640.17] - Subpart B—Red Blood Cells
Subpart C [§ 640.20 - § 640.25] - Subpart C—Platelets
Subpart D [§ 640.30 - § 640.34] - Subpart D—Plasma
Subpart E - Subpart E [Reserved]
Subpart F [§ 640.50 - § 640.56] - Subpart F—Cryoprecipitate
Subpart G [§ 640.60 - § 640.76] - Subpart G—Source Plasma
Subpart H [§ 640.80 - § 640.84] - Subpart H—Albumin (Human)
Subpart I [§ 640.90 - § 640.94] - Subpart I—Plasma Protein Fraction (Human)
Subpart J [§ 640.100 - § 640.104] - Subpart J—Immune Globulin (Human)
Subpart K - Subpart K [Reserved]
Subpart L [§ 640.120 - § 640.120] - Subpart L—Alternative Procedures
Subpart M [§ 640.125 - § 640.130] - Subpart M—Definitions and Medical Supervision
authority:
21 U.S.C. 321
,
351
,
352
,
353
,
355
,
360
,
371
;
42 U.S.C. 216
,
262
,
263
,
263
a,
264
source:
38 FR 32089, Nov. 20, 1973, unless otherwise noted.
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