OpenClinica

Insight turns operational and clinical data into graphical reports built to customer specifications.

The page describes eConsent as an electronic consent tool for creating multimedia, dynamic experiences for clinical trial participants.

OpenClinica leads the new generation of electronic patient reported outcomes, enabling patients to report their data on any mobile device.

OpenClinica offers integrated randomization for clinical trials.

An OpenClinica case study offers lessons learned for migrating active studies to a new EDC

Managing the complexities of informed consent by legally authorized representatives (LAR) in clinical trials.

OpenClinica's blog covers trends, topics, and tips for improving clinical trials.

The post discusses efforts to reduce the costs and barriers of integrating eClinical applications and data, including a LinkedIn discussion among software vendors and industry experts.

The page lists pricing for eClinical tools, including EDC, eConsent, eCOA, and randomization. Plans scale for academic, CRO, and sponsor teams and include a free expert study build.

The page compares OpenClinica Community, Enterprise (OC3.x), and OC4 versions in summary and feature-by-feature tables.

The page compares REDCap with OpenClinica Study Hub, which combines participant recruitment, engagement, enrollment, and clinical data capture in a connected workflow.

The page introduces the team responsible for OpenClinica and its customers' data experiences.

Cost-effective EDC, ePRO and Randomization from OpenClinica ensure higher quality data, which is crucial for trials of every size and scope.

The page answers frequently asked questions about open source, EDC, and OpenClinica's Community edition.

The page offers technical support, free trials, and conversations with the company.

The page lists clinical trial technology services, including eSource, EDC, ePRO, eConsent, eCOA, randomization, reporting, and rescue study services.