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CTTI

Clinical Trials Transformation Initiative

Study Operations

Executive Summary: CTTI Recommendations for Efficient and Effective Clinical Trial Recruitment Planning

Posted on August 4, 2021February 10, 2025 by Hannah Faulkner

Executive Summary: CTTI Recommendations for Efficient and Effective Clinical Trial Recruitment Planning

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

Best Practices for Designing High-Quality, Diverse COVID-19 Trials

Posted on July 9, 2021February 21, 2025 by Hannah Faulkner

Best Practices for Designing High-Quality, Diverse COVID-19 Trials

Posted in Access to Clinical Trials, COVID 19, COVID-19, Ensuring Quality, Innovative Trials, Regulatory Submissions + Approvals, Related: COVID 19, Resources, Study Design, Study Operations

Best Practices for Conducting Trials during the COVID-19 Pandemic

Posted on July 9, 2021February 21, 2025 by Hannah Faulkner

Best Practices for Conducting Trials during the COVID-19 Pandemic

Posted in Access to Clinical Trials, COVID 19, COVID-19, Ensuring Quality, Innovative Trials, Regulatory Submissions + Approvals, Related: COVID 19, Resources, Study Design, Study Operations

Digital Health Trials: Recommendations for Managing Data

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

Digital Health Trials: Recommendations for Managing Data

Posted in Data Collecting and Reporting, Innovative Trials, Managing Data, Managing Data, Recommendations, Study Design, Study Operations

Study Start-Up Timelines: Identifying Challenges & Opportunities for Change

Posted on July 6, 2021February 20, 2025 by Hannah Faulkner

Study Start-Up Timelines: Identifying Challenges & Opportunities for Change

Posted in Related: Study Start-Up, Site Planning, Study Operations, Study Start-Up, Study Start-Up

Feasibility Studies Database

Posted on June 30, 2021February 11, 2025 by Hannah Faulkner

Feasibility Studies Database

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

Single IRB: Determination of Institutional Engagement Overview

Posted on June 25, 2021February 11, 2025 by Hannah Faulkner

Single IRB: Determination of Institutional Engagement Overview

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

Informed Consent Discussion Tool

Posted on June 25, 2021February 5, 2025 by Hannah Faulkner

Informed Consent Discussion Tool

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

sIRB Flowchart: Determining Engagement of Institutions in Research

Posted on June 25, 2021February 11, 2025 by Hannah Faulkner

sIRB Flowchart: Determining Engagement of Institutions in Research

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

Master Protocol Studies: Emerging Best Practices to Drive Multi-Stakeholder Collaboration & Mobilization

Posted on June 24, 2021February 6, 2025 by Hannah Faulkner

Master Protocol Studies: Emerging Best Practices to Drive Multi-Stakeholder Collaboration & Mobilization

Posted in Innovative Trials, Master Protocol Studies, Master Protocols, Resources, 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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