Clinical Trial Management

Eliminate ambiguity between clinicians and developers. Learn how Gherkin and 'living documentation' are streamlining trial deployments.

Impacting a small percentage of the population yet affecting millions of individuals worldwide, rare diseases pose distinct challenges for

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.

The Belmont Report, issued in 1979 by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral

The process of submitting participant materials to Institutional Review Boards (IRBs) in the United States and Ethics

The United Nations’ Resolution on Persons Living with a Rare Disease, adopted on December 16, 2021, marks a

The success of a clinical trial hinges on the active involvement and retention of its participants

A cornerstone of medical progress, clinical trials lead to treatments and innovations that improve the lives of

In the ever-evolving landscape of clinical research, innovative strategies are crucial to streamline