Blog

Clinical Trial Management

Experience the future of research through a digital-first lens. We break down how AI, ePROs, and integrated platforms are redefining clinical trials to accelerate development and improve patient outcomes.

Clinical Trial Management

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

Clinical Trial Management

Why Digital-First ePRO and eCOA Are Now Essential to Modern Clinical Trials

Electronic Patient-Reported Outcomes (ePRO) have moved far beyond being a digital replacement for paper. In today’s decentralized, hybrid, and globally distributed trials, ePRO and broader eCOA capabilities have become foundational to high-quality data collection, participant safety, protocol compliance, and operational efficiency.

Clinical Trial Management

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

Clinical Trial Management

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

Clinical Trial Management

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

Clinical Trial Management

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

Clinical Trial Management

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