“The responsiveness and ability to help us get our studies set up quickly while meeting stringent UK validation requirements drove our decision to use OpenClinica."
Waltham, MA (PRWEB) March 26, 2014
OpenClinica, LLC announces that Research in Real-Life (RiRL) has selected the OpenClinica Enterprise Edition electronic data capture (EDC) and clinical data management system (CDMS) to support a wide range of clinical research, ranging from medical device, interventional, and investigator lead studies. With offices in Singapore and Cambridge, UK, RiRL is a boutique CRO that collaborates with clinical, academic and industry partners to standardize optimal real-life research methods and ensure effective dissemination of real-life data.
Professor David Price, owner and director at RiRL commented, “The responsiveness and ability to help us get our studies set up quickly while meeting stringent UK validation requirements drove our decision to use OpenClinica." Jo Steele, Data Manager at RiRL added, “From the very first contact to an ad hoc vendor audit, it became clear that OpenClinica was the correct choice.”
The OpenClinica software is available in two editions. The OpenClinica Community Edition is freely available under the LGPL open source license. The OpenClinica Enterprise Edition offers a full suite of services including Central User Training, expert Client Support, optimized hosting and critical regulatory validation support documentation and automated testing.
Research in Real-Life (RiRL) is an independent, research-driven organization, established to cultivate initiatives, provide evidence, and drive quality standards within the growing field of real-life, pragmatic research. RiRL’s research activities contribute to the pre- and post-marketing assessment of therapeutic interventions and help drive the current paradigm shift in healthcare evaluation towards inclusion of real-life data. For more information, visit http://rirl.org.
About OpenClinica, LLC
OpenClinica, LLC enhances the productivity of clinical trials through commercial open source software. With thousands of implementations at biopharmaceutical companies, contract research organizations, academic, and government organizations worldwide, the OpenClinica software facilitates electronic data capture and data management, increasing the speed of collection and quality of data in clinical trials. OpenClinica supports HIPAA, 21 CFR Part 11, and other regulatory guidelines and is designed as a standards-based, extensible, and modular platform. For more information, visit https://www.openclinica.com.