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We found 16 resources that match your search.

Creating a New Submission in the DPRS Quick Reference Cardpdf

Quick reference card for creating a new submission in the DPRS.

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DAIDS Deregistrationpdf

Guidance regarding the DAIDS deregistration process.

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DAIDS Financial Disclosure Guidancepdf

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

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DAIDS Investigator of Record (IoR) Formpdf

DAIDS investigator of record form (7/2020).

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DAIDS Protocol Registration Basic Trainingpdf

DAIDS protocol registration basic training.

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DAIDS Protocol Specific Informed Consent Template - General Use

Informed Consent documents are in the process of being updated to be compliant with the revised Common Rule.

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DAIDS RSC PRO Timelinespdf

DAIDS protocol registration timelines.

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Financial Disclosure Form for Non-networkspdf

Non-network financial disclosure/certification form.

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Financial Disclosure Forms for ACTGzip

AIDS clinical trials group network IND study financial disclosure form. .zip file includes ACTG Network IND Study Financial Disclosure Form (PDF) ACTG Network IND Study Financial Disclosure Form Template (PDF) ACTG Network IND Study Financial Disclosure Form Fillable (PDF)  

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Instructions Page for the DAIDS Protocol Specific Informed Consent Template 2/23/2016

Informed Consent documents are in the process of being updated to be compliant with the revised Common Rule.

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Instructions Page for the DAIDS Protocol Specific Informed Consent Template 7/24/2013

DAIDS protocol specific informed consent template—general use.

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Protocol Registration at a Glance Quick Reference Cardpdf

Quick reference card for protocol registration at a glance.

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Protocol Registration Checklistpdf

Division of AIDS (DAIDS) protocol registration checklist. NOTE: This form is not required if submitting materials through the DAIDS Protocol Registration System (DPRS).

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Protocol Registration Checklist (Alternate Format)doc

Division of AIDS (DAIDS) protocol registration checklist. NOTE: This form is not required if submitting materials through the DAIDS Protocol Registration System (DPRS).

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Required Documentation Based on 45 CFR 46pdf

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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Translation Confirmation Documentpdf

DAIDS protocol registration translation confirmation document.

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