CliniOps moves to a new home
CliniOps moved to its new US office in Fremont. The office is centrally located close to Fremont hub: 38750 Paseo Padre Parkway, Suite C8, Fremont, CA – 94536, USA. Our new home will accommodate CliniOps’s growing team for the next year, and beyond. It is also equipped with the latest audio-video connectivity to provide the highest level of support to its growing international customers base.
Quarterly Updates Apr – Jun 2017
KPMG completes review of CliniOps Quality & Security Management Framework
CliniOps invited KPMG to review its Quality and Security Management framework. The exercise started earlier this year and was successfully completed this quarter.
Everest Group featured CliniOps in its report
Everest Group recognizes CliniOps among ‘five hottest startups driving digital disruption in the life sciences industry’, in its research publication “Hot Life Sciences Startups: Friends, Foes, and Frenemies in the Innovation Ecosystem”, April 10, 2017
CliniOps invited by CURhE at the PAS Conference
CliniOps invited to Pediatric Academic Societies (PAS) 2017 conference, as part of the CURhE team, in San Francisco, May 7, 2017.
Innovation That Matters
Multi-lingual Support for Global Studies
Majority of the clinical trials are very global in nature. Most Phase 3 clinical trials are usually run at trial sites spread across US, Africa, Asia, EU and South America. Hence, multi-lingual support becomes very essential to support such diverse nature of clinical trials. As part of the patient enrollment process, its is mandatory that patients are explained property (in a language that they understand) about the risks and benefits of the trials. On the same token, the site coordinators, many of whom may only understand the local language, also needs to be empowered with the language translation of the CRF forms, so they collect the appropriate data and ensures clean data collection.
Having supported trials all across Americas, Africa, Asia etc, CliniOps eSource solution can support any local language as needed per the study protocol.
Medical Device Integration with eSource solution, ensuring high quality data at source
Most clinical trials invariable collects certain data that comes from medical devices. these device data is usually manually transcribed into the Data collection software, which often times, results in transcription errors. Such errors can easily be eliminated if data from medical devices can seamlessly be ported into the Data collection software.
CliniOps eSource solution provides the capability to seamlessly integrate with several medical devices, typically with bluetooth technology. The medical devices are paired with the right tablets and data is passed seamlessly to the right field in the CRF forms.
Awards & Recognition
Frost & Sullivan Technology Leadership Award, 2017
CliniOps receives the ‘2017 Frost & Sullivan Technology Leadership Award for Digitalization of Clinical Trials’