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Section 607.3
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Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products |
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Section 607.7
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Who must register and submit a blood product list |
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Section 607.20
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Times for establishment registration and blood product listing |
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Section 607.21
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How and where to register establishments and list blood products |
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Section 607.22
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Information required for establishment registration and blood product listing |
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Section 607.25
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Amendments to establishment registration |
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Section 607.26
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Updating blood product listing information |
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Section 607.30
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Additional blood product listing information |
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Section 607.31
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Notification of registrant; blood product establishment registration number and NDC Labeler Code |
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Section 607.35
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Inspection of establishment registrations and blood product listings |
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Section 607.37
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Misbranding by reference to establishment registration or to registration number |
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Section 607.39
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Establishment registration and blood product listing requirements for foreign blood product establishments |
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Section 607.40
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Exemptions for blood product establishments |
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Section 607.65
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Tests prior to release required for each lot |