Title 21--Food and Drugs

CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES--(Continued)

PART 640--ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS


TEXT PDF640.1 Whole Blood.
TEXT PDF640.2 General requirements.
TEXT PDF640.3 Suitability of donor.
TEXT PDF640.4 Collection of the blood.
TEXT PDF640.5 Testing the blood.
TEXT PDF640.6 Modifications of Whole Blood.
TEXT PDF640.10 Red Blood Cells.
TEXT PDF640.11 General requirements.
TEXT PDF640.12 Suitability of donor.
TEXT PDF640.13 Collection of the blood.
TEXT PDF640.14 Testing the blood.
TEXT PDF640.15 Pilot samples.
TEXT PDF640.16 Processing.
TEXT PDF640.17 Modifications for specific products.
TEXT PDF640.20 Platelets.
TEXT PDF640.21 Suitability of donors.
TEXT PDF640.22 Collection of source material.
TEXT PDF640.23 Testing the blood.
TEXT PDF640.24 Processing.
TEXT PDF640.25 General requirements.
TEXT PDF640.27 Emergency provisions.
TEXT PDF640.30 Plasma.
TEXT PDF640.31 Suitability of donors.
TEXT PDF640.32 Collection of source material.
TEXT PDF640.33 Testing the blood.
TEXT PDF640.34 Processing.
TEXT PDF640.50 Cryoprecipitated AHF.
TEXT PDF640.51 Suitability of donors.
TEXT PDF640.52 Collection of source material.
TEXT PDF640.53 Testing the blood.
TEXT PDF640.54 Processing.
TEXT PDF640.55 U.S. Standard preparation.
TEXT PDF640.56 Quality control test for potency.
TEXT PDF640.60 Source Plasma.
TEXT PDF640.61 Informed consent.
TEXT PDF640.62 Medical supervision.
TEXT PDF640.63 Suitability of donor.
TEXT PDF640.64 Collection of blood for Source Plasma.
TEXT PDF640.65 Plasmapheresis.
TEXT PDF640.66 Immunization of donors.
TEXT PDF640.67 Laboratory tests.
TEXT PDF640.68 Processing.
TEXT PDF640.69 General requirements.
TEXT PDF640.70 Labeling.
TEXT PDF640.71 Manufacturing responsibility.
TEXT PDF640.72 Records.
TEXT PDF640.73 Reporting of fatal donor reactions.
TEXT PDF640.74 Modification of Source Plasma.
TEXT PDF640.76 Products stored or shipped at unacceptable temperatures.
TEXT PDF640.80 Albumin (Human).
TEXT PDF640.81 Processing.
TEXT PDF640.82 Tests on final product.
TEXT PDF640.83 General requirements.
TEXT PDF640.84 Labeling.
TEXT PDF640.90 Plasma Protein Fraction (Human).
TEXT PDF640.91 Processing.
TEXT PDF640.92 Tests on final product.
TEXT PDF640.93 General requirements.
TEXT PDF640.94 Labeling.
TEXT PDF640.100 Immune Globulin (Human).
TEXT PDF640.101 General requirements.
TEXT PDF640.102 Manufacture of Immune Globulin (Human).
TEXT PDF640.103 The final product.
TEXT PDF640.104 Potency.
TEXT PDF640.120 Alternative procedures.


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