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CTTI

Clinical Trials Transformation Initiative

Study Operations

Framework: Specifications to Consider During Digital Health Technology Selection

Posted on June 7, 2021February 11, 2025 by Hannah Faulkner

Framework: Specifications to Consider During Digital Health Technology Selection

Posted in Digital Health Technologies, Digital Health Trials, Innovative Trials, Resources, Selecting and Testing Digital Health Technology, Study Operations

Recommendations for Using Single IRBs (sIRB) for Multicenter Clinical Trials

Posted on June 7, 2021July 3, 2025 by Hannah Faulkner

Recommendations for Using Single IRBs for Multicenter Clinical Trials

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

Recommendations for Advancing the Use of Single IRBs (sIRB) for Multicenter Clinical Trials

Posted on June 7, 2021July 3, 2025 by Hannah Faulkner

Recommendations for Advancing the Use of Single IRBs for Multicenter Clinical Trials

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

Recommendations for IND Safety Assessment and Communication

Posted on June 7, 2021February 11, 2025 by Hannah Faulkner

Recommendations for IND Safety Assessment and Communication

Posted in Recommendations, SAE Reporting, Safety, Safety Reporting, Study Operations

Recommendations for Desired Attributes of Electronic Portals for Expedited Safety Reporting

Posted on June 7, 2021February 11, 2025 by Hannah Faulkner

Recommendations for Desired Attributes of Electronic Portals for Expedited Safety Reporting

Posted in Recommendations, SAE Reporting, Safety, Safety Reporting, Study Operations

How to Identify and Prioritize Trial Stakeholders

Posted on June 7, 2021February 10, 2025 by Hannah Faulkner

How to Identify and Prioritize Trial Stakeholders

Posted in Ensuring Quality, Recruitment, Recruitment, Recruitment, Resources, Study Design, Study Operations

Should I Include Patient Reported Outcomes (PROs) in my Study?

Posted on June 7, 2021February 10, 2025 by Hannah Faulkner

Should I Include Patient Reported Outcomes (PROs) in my Study?

Posted in Ensuring Quality, Recruitment, Recruitment, Recruitment, Resources, Study Design, Study Operations

How to Monitor Recruitment Process and Performance

Posted on June 7, 2021February 10, 2025 by Hannah Faulkner

How to Monitor Recruitment Process and Performance

Posted in Ensuring Quality, Recruitment, Recruitment, Recruitment, Resources, Study Design, Study Operations

Decision Tree: Optimizing Your Protocol Design

Posted on June 7, 2021February 10, 2025 by Hannah Faulkner

Decision Tree: Optimizing Your Protocol Design

Posted in Ensuring Quality, Recruitment, Recruitment, Recruitment, Resources, Study Design, Study Operations

Recommendations for Planning for Successful Trial Recruitment

Posted on June 7, 2021February 10, 2025 by Hannah Faulkner

Recommendations for Planning for Successful Trial Recruitment

Posted in Ensuring Quality, Recommendations, Recruitment, Recruitment, Recruitment, Study Design, Study Operations

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DISCLAIMER: CTTI encourages the use of all materials listed on this site in the pursuit of improving the clinical trials enterprise. Our recommendations, tools, meeting summaries, and more are available to the public for free. We do ask that you acknowledge the source whenever using or referencing CTTI materials. Read our Citation Policy. 

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