7348.003 |
In Vivo Bioavailability-Bioequivalence Studies - Clinical |
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PDF |
7348.004 |
In Vivo Bioavailability-Bioequivalence Studies - Analytical |
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PDF |
7348.007 |
Inspection of Nonclinical Laboratories Conducting Animal Rule-Specific Studies |
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PDF |
7348.808 |
Good Laboratory Practice (Nonclinical Laboratories) |
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PDF(117 kb) |
7348.808A |
Good Laboratory Practice Program (Nonclinical Laboratories) EPA Data Audit Inspections |
HTML |
PDF(38 kb) |
7348.809 |
Institutional Review Board |
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PDF(293 kb) |
7348.809A |
Radioactive Drug Research Committee |
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PDF (155 kb) |
7348.810 |
Sponsors and Contract Research Organizations |
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PDF |
7348.811 |
Clinical Investigators and Sponsor-Investigators |
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PDF |
7353.001 |
Postmarketing Adverse Drug Experience (PADE) Reporting Inspections |
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PDF (335 kb) |
7353.001C |
Risk Evaluation and Mitigation Strategies (REMS) Reporting Inspections |
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PDF |