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Lists of IND and non-IND protocols having case report forms (CRFs) and pharmacy records that will not be stored by DAIDS .

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Guidance regarding the DAIDS deregistration process.

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Process for collection of financial disclosure by clinical investigators conducting DAIDS-sponsored IND trials.

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Guidance and requirements for daids-supported research involving recombinant DNA.

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List of IND protocols having CRF/Pharmacy records that will not be stored by DAIDS.

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Instructions for the transfer of case report forms, (CRF) and pharmacy records to the DAIDS regulatory support center, (DAIDS RSC).

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Completed Non-IND studies that have met or exceeded the 3 year retention period (per 45 CFR 46.115); CRFs and pharmacy records will not be stored by DAIDS.

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Required documentation of risk/benefit category and approval of clinical studies for inclusion of children by institutional review boards/ethics committees based on 45 CFR 46, Subpart D.

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