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2020 IND Lists of Studies having CRF/Pharmacy Records That Will Not be Stored by DAIDS

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2020 non-IND Lists of Studies having CRF/Pharmacy Records That Will Not be Stored by DAIDS

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Algorithm for Determining Whether Site Specific Informed Consent Forms will be Reviewed at the Time of Initial Protocol Registration

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DAIDS Memo Regarding Timing of Consent and Re-Consent with Updated IRB/EC/RE-Approved Informed Consent Forms

DAIDS Memo Regarding Timing of Consent and Re-Consent with Updated IRB/EC/RE-Approved Informed Consent Forms.

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DAIDS Protocol Change Process Job Aid

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DAIDS Protocol Change Process Policy

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Guidelines for Electronic Submissions Via Email-EPR Guidelines

Guidelines for Electronic Submissions Via Email-EPR Guidelines

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How to Initiate the ClinicalTrials.gov Initial Registration Process Memorandum

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Instructions for Authorization and Transfer of CRFs and Pharmacy Records to the DAIDS RSC

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Memorandum— DAIDS ClinicalTrials.gov Protocol Checklist

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Monthly Comprehensive Safety Distribution Report (CSDR) FAQ

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