| Section 52-3.1 - Compliance with FDA regulations and manufacturers' instructions |
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| Section 52-3.2 - Sterilization of instruments |
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| Section 52-3.3 - Qualifications of donors |
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| Section 52-3.5 - Quality assurance and safety requirements |
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| Section 52-3.6 - HIV antibody testing and notification |
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| Section 52-3.7 - Reporting requirements |
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| Section 52-3.8 - Special circumstances |
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