We are passionate about helping our partners effectively monitor and control their clinical trials for better, faster, more accurate results. Below are some of our key partners:
Fresh Gravity is a business and technology consulting firm that assists enterprises with their digital transformation journey by using state-of-the-art technologies. Our core strengths lie in Enterprise Data Management, Data Engineering, Data Science, Artificial Intelligence and Enterprise Integration. Fresh Gravity clinical data experts have decades of hands-on experience helping Pharma companies and CROs implement technology solutions to solve complex data and analytics problems making us uniquely qualified to help our customers solve their clinical data problems.
For more information, visit www.freshgravity.com
JSS Medical Research is a full-service clinical research organization (CRO) with strong academic affiliations offering a wide range of services internationally. One of our distinguishing attributes is our methodological knowledge and expertise in the design and execution of clinical studies. These include all phases of development such as Phase I, II and III, and post-approval studies. The breadth of our experience enables our clients to collaborate with the same partner throughout the product lifecycle.
For more information visit www.jssresearch.com
At Medrio, we know it takes a village to achieve clinical trial breakthroughs. Our full-service eClinical Data Management solutions and white-glove customer service have helped secure over 375 approvals for global CROs, sponsors, and sites across the life sciences spectrum. Discover the Medrio difference at medrio.com.
Navitas, the dedicated life sciences company of TAKE Solutions, harnesses the combined knowledge and experience of three legacy companies—Ecron Acunova, Navitas, and Intelent—to provide end-to-end services and solutions. We help our clients address their most critical problems by bringing together the capabilities of a full-service CRO, a technology-led life sciences services provider across clinical, regulatory and safety, and a life sciences big data services and analytics provider.
ThoughtSphere powers the Navitas OneClinical platform. For more information visit http://www.navitaslifesciences.com/oneclinical
Signant Health is the evidence generation company. We are focused on leveraging software, deep therapeutic and scientific knowledge, and operational expertise to consistently capture, aggregate, and reveal quality evidence for clinical studies across traditional, virtual, and hybrid trial models. For more than 20 years, over 400 sponsors and CROs of all sizes – including all Top 20 pharma – have trusted Signant solutions for remote and site-based eCOA, eConsent, RTSM, supply chain management, and data quality analytics. Learn more at www.signanthealth.com.
With 800 staff members across 21 countries, Synteract is an innovative, full-service contract research organization supporting biopharmaceutical companies in all phases of clinical development to help bring new medicines to market. Synteract has conducted nearly 4,000 studies on six continents and in more than 60 countries, working with more than 26,000 investigative sites and nearly 750,000 patients. It has contributed to more than 240 product approvals. The CRO offers a notable depth of expertise in its centers of development in oncology and neuro-degenerative indications, as well as rare and orphan, pediatric, and immunotherapy studies, and now dermatology.
ThoughtSphere powers the Synteract Insights data aggregation platform. For more information visit www.synteract.com/Services/Clinical-Technology
With more than 17 years of experience, global reach, and clients ranging from diagnostic start-ups to international pharmaceuticals, CROs to consultancies, TrialStat Solutions, Inc. is at the forefront of a new paradigm in life sciences technology, delivering integrated, flexible, and easily implemented on-demand data management and reporting solutions.
TrialStat’s eClinical Suite consists of a fully unified product offering including EDC, Randomization, ePRO, Adjudication, Coding, AE/SAE Management, Vendor Neutral Image Archive, CTMS and a robust Reporting and Analytics Portal. We stand alone in the industry with such an all-compassing suite of products for conducting clinical trials that can also be seamlessly connected to external data sources such as EMR, mobile devices and wearables, imaging, data warehousing, and other Clinical and non-clinical data and information sources.