Ethical GmbH Improves Its eClinical Software with PrizmDoc Viewer Redaction & Annotation APIs

In the process of building eAdjudication, Ethical recognized a need for a document viewer that specializes in secure redaction technology. In fact, the Endpoint Adjudication process requires that a panel of experts examine the data and documents related to a specific clinical event and express a judgement on it. The experts must assess the data in a blind and independent way, without any bias on the trial context or patient background.

About the Client

Beginning as eClinical developers, our staff gained experience spanning the range of the eClinical world: eClinical technology, clinical systems, and data management in global trials, clinical trial quality and data compliance, and of course, endpoint adjudication (EA). We gained the experience in successful engagements with academic research organizations (AROs), biopharmaceutical or medical device enterprises, clinical research organizations (CROs), and independent review committees. We have become expert in the creation, performance, and management of the EA process workflows and forms validation, private health information management and compliance, clinical trial and GxP compliance, clinical systems design, integration and management, as well as web and mobile interface design.

Ethical GmbH Logo
When we first started looking for a redaction tool, we researched several different companies. We compared Accusoft to a company in Europe, and concluded that Accusoft is the most experienced and advanced solution for APIs.
Mimmo Garibbo, Director and Founder, Ethical GmbH
Ethical GmbH Case Study
Accusoft's PrizmDoc Viewer APIs help Ethical GmbH redact sensitive information from clinical trials. The PrizmDoc annotation and redaction APIs are useful for panel review. Endpoint adjudication requires a panel of experts to examine data from clinical trials securely before expressing judgment.
To learn more, download the full case study. Download Now