Resources

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Harnessing the Power of Behavior-Driven Development in Clinical Trials

Clinical trials are the backbone of medical research, paving the way for innovative treatments and therapies. Yet, they often encounter delays, errors, and inefficiencies. Enter […]

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Clinical trials are the backbone of medical research, paving the way for innovative treatments and therapies. Yet, they often encounter delays, errors, and inefficiencies. Enter

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Joseph Farrell

October 23, 2024

The High Cost of Clinical Trial Platforms: A Barrier to Rare Disease Research

Impacting a small percentage of the population yet affecting millions of individuals worldwide, rare diseases pose distinct challenges for medical research. While eClinical trial platforms

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Impacting a small percentage of the population yet affecting millions of individuals worldwide, rare diseases pose distinct challenges for medical research. While eClinical trial platforms

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Joseph Farrell

March 13, 2024

Advancing Data Collection: ePROs vs Traditional Paper Methods in Patient-Reported Outcomes

Electronic Patient-Reported Outcomes (ePROs) have increasingly become the preferred method for collecting participant data in clinical trials and healthcare settings, surpassing traditional paper-based Patient-Reported Outcomes

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Electronic Patient-Reported Outcomes (ePROs) have increasingly become the preferred method for collecting participant data in clinical trials and healthcare settings, surpassing traditional paper-based Patient-Reported Outcomes

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Joseph Farrell

January 9, 2024

The Enduring Influence of the Belmont Report on Policy and Participant Safety

The Belmont Report, issued in 1979 by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, is a foundational document

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The Belmont Report, issued in 1979 by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, is a foundational document

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Joseph Farrell

December 26, 2023

IRB Submission Strategies in the United States and the European Union

The process of submitting participant materials to Institutional Review Boards (IRBs) in the United States and Ethics Committees (ECs) in the European Union is a

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The process of submitting participant materials to Institutional Review Boards (IRBs) in the United States and Ethics Committees (ECs) in the European Union is a

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Joseph Farrell

December 9, 2023

Bridging the Gaps: The United Nations’ Resolution on Rare Disease

The United Nations’ Resolution on Persons Living with a Rare Disease, adopted on December 16, 2021, marks a significant milestone in global health policy. This

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The United Nations’ Resolution on Persons Living with a Rare Disease, adopted on December 16, 2021, marks a significant milestone in global health policy. This

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Joseph Farrell

November 28, 2023

Elevating Engagement and Retention in Clinical Trials with Digital Solutions

The success of a clinical trial hinges on the active involvement and retention of its participants. Yet the challenge of engagement remains a pressing concern

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The success of a clinical trial hinges on the active involvement and retention of its participants. Yet the challenge of engagement remains a pressing concern

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Joseph Farrell

November 6, 2023

Transforming Rare Disease Clinical Trials: The Power of Digital Platforms

A cornerstone of medical progress, clinical trials lead to treatments and innovations that improve the lives of countless people suffering from a wide range of

Transforming Rare Disease Clinical Trials: The Power of Digital Platforms Read More »

A cornerstone of medical progress, clinical trials lead to treatments and innovations that improve the lives of countless people suffering from a wide range of

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Joseph Farrell

November 3, 2023