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321. Chemistry, manufacturing, and control (CMC) information for human gene therapy investigational new drug applications (INDs)

323. Testing of retroviral vector-based human gene therapy products for replication competent retrovirus during product manufacture and patient follow-up

325. Human gene therapy for hemophilia

327. Use of serological tests to reduce the risk of transfusion-transmitted human T-lymphotropic virus types I and II (HTLV-I/II)

330. Recommendations for clinical laboratory improvement amendments of 1988 (CLIA) waiver applications for manufacturers of in vitro diagnostic devices: guidance for industry and Food and Drug Administration staff