Title 21

PART 630

Part 630 - Requirements For Blood And Blood Components Intended For Transfusion Or For Further Manufacturing Use

PART 630 - REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE Authority:21 U.S.C. 321, 331, 351, 352, 355, 360, 371; 42 U.S.C. 216, 262, 264. Source:66 FR 31176, June 11, 2001, unless otherwise noted.

• Authority: 21 U.S.C. 321, 331, 351, 352, 355, 360, 371; 42 U.S.C. 216, 262, 264.
• Source: 66 FR 31176, June 11, 2001, unless otherwise noted.

21:7.0.1.1.6.1	SUBPART A	Subpart A - General Provisions
21:7.0.1.1.6.1.1.1	SECTION 630.1	630.1 Purpose and scope.
21:7.0.1.1.6.1.1.2	SECTION 630.3	630.3 Definitions.
21:7.0.1.1.6.2	SUBPART B	Subpart B - Donor Eligibility Requirements
21:7.0.1.1.6.2.1.1	SECTION 630.5	630.5 Medical supervision.
21:7.0.1.1.6.2.1.2	SECTION 630.10	630.10 General donor eligibility requirements.
21:7.0.1.1.6.2.1.3	SECTION 630.15	630.15 Donor eligibility requirements specific to Whole Blood, Red Blood Cells and Plasma collected by apheresis.
21:7.0.1.1.6.2.1.4	SECTION 630.20	630.20 Exceptions for certain ineligible donors.
21:7.0.1.1.6.2.1.5	SECTION 630.25	630.25 Exceptions from certain donor eligibility requirements for infrequent plasma donors.
21:7.0.1.1.6.2.1.6	SECTION 630.30	630.30 Donation suitability requirements.
21:7.0.1.1.6.2.1.7	SECTION 630.35	630.35 Requalification of previously deferred donors.
21:7.0.1.1.6.3	SUBPART C	Subpart C - Donor Notification
21:7.0.1.1.6.3.1.1	SECTION 630.40	630.40 Requirements for notifying deferred donors.

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