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CTTI

Clinical Trials Transformation Initiative

Resources

CTTI Advancing the Use of Single IRBs for Multicenter Clinical Trials: Template IRB Authorization Agreement

Posted on June 8, 2021February 11, 2025 by Hannah Faulkner

CTTI Advancing the Use of Single IRBs for Multicenter Clinical Trials: Template IRB Authorization Agreement

Posted in Resources, Safety, Single IRB, Single IRB, Study Operations

Evaluation Framework for the NIH Single IRB Policy

Posted on June 8, 2021February 11, 2025 by Hannah Faulkner

Evaluation Framework for the NIH Single IRB Policy

Posted in Resources, Safety, Single IRB, Single IRB, Study Operations

Single IRB: Resource of Resources Document

Posted on June 8, 2021February 11, 2025 by Hannah Faulkner

Single IRB: Resource of Resources Document

Posted in Resources, Safety, Single IRB, Single IRB, Study Operations

Framework of Characteristics of a Qualified Site Team: How Does Yours Measure Up?

Posted on June 8, 2021February 6, 2025 by Hannah Faulkner

Framework of Characteristics of a Qualified Site Team: How Does Yours Measure Up?

Posted in Investigator Qualification, Investigator Qualification, Resources, Site Planning, Study Operations

Instructions for Documenting Qualification Activities

Posted on June 8, 2021February 6, 2025 by Hannah Faulkner

Instructions for Documenting Qualification Activities

Posted in Investigator Qualification, Investigator Qualification, Resources, Site Planning, Study Operations

Documenting Qualification: A Quick-Reference Guide for Investigators and their Delegates

Posted on June 8, 2021February 6, 2025 by Hannah Faulkner

Documenting Qualification: A Quick-Reference Guide for Investigators and their Delegates

Posted in Investigator Qualification, Investigator Qualification, Resources, Site Planning, Study Operations

Sample Tiered Informed Consent Model

Posted on June 8, 2021February 5, 2025 by Hannah Faulkner

Sample Tiered Informed Consent Model

Posted in Informed Consent, Informed Consent, Resources, Safety, Study Design, Study Operations

Informed Consent Training Resources

Posted on June 8, 2021February 5, 2025 by Hannah Faulkner

Informed Consent Training Resources

Posted in Informed Consent, Informed Consent, Resources, Safety, Study Design, Study Operations

Evaluating Feasibility of RWD-Supported Recruitment

Posted on June 8, 2021February 10, 2025 by Hannah Faulkner

Evaluating Feasibility of RWD-Supported Recruitment

Posted in Real World Data, Recruitment, Resources, RWD for Eligibility and Recruitment, Site Planning, Study Design

Effective RWD-Supported Discussions of Eligibility Criteria

Posted on June 8, 2021February 10, 2025 by Hannah Faulkner

Effective RWD-Supported Discussions of Eligibility Criteria

Posted in Real World Data, Recruitment, Resources, RWD for Eligibility and Recruitment, Site Planning, Study Design

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