CliniOps is a Silicon-Valley based startup, founded in 2013 with a mission to enable complete digitalization of clinical trials, drug safety, and patient care.
2016 has been a tremendous growth year for CliniOps. The company started commercializing its solutions this year and within a year it has achieved several important milestones. CliniOps established and grew its operations and successfully supported first premarket submission to FDA – 510(K) for a client, and several other studies in progress.
Quarterly Updates Oct – Dec 2016
Frost & Sullivan featured CliniOps in its report
CliniOps featured in Frost & Sullivan’s recent analyst report on ‘Emerging Technologies Energizing the Future of the Pharmaceutical Sector’ in the ‘Cloud Platform Enabling The Digitization Of Clinical Trials’ section, published on
September 28, 2016
Arjun Malhotra Joins CliniOps Board of Advisors
Arjun is a pioneer of the Indian IT industry. He was the Chairman of Headstrong, before its acquisition by Genpact. He started his illustrious career as a co-founder of the HCL group in 1975, taking it from a six-person “garage operation” to a multi-billion global organization. He is presently an Advisor in a number of start-ups in Education and healthcare space.
CliniOps eSource solution in COR-NTD Conference 2016
Joshua Bogus, Project Manager for the DOLF (Death to Onchocerciasis and Lymphatic Filariasis) project, supported by the Bill and Melinda Gates Foundation, presented the CliniOps eSource solution, at the COR-NTD (Coalition for Operational Research on Neglected Tropical Disease) Conference, Atlanta, Nov 2016.
Stanford Invited CliniOps Team
CliniOps team was invited to present their work to a group of physicians, faculty members, researchers and students as part of the Stanford NeoDesign Speaker Series, Department of Pediatrics.
CliniOps Established A New Partnership
CliniOps entered into a new partnership agreement with a $16 Billion Global services firm with a significant Life Sciences focus, servicing 7 of the top 10 Pharma companies.
Innovation That Matters
eConsent Revolutionizing The Registration Process
The current process of documenting consent on paper meant that it took a lot of time to register the patients and resulted in a cumbersome paperwork reducing the efficiency. CliniOps introduced the FDA compliant eConsent procedure which helped our clients register the required patients in record time, while making it really easy to manage and archive Informed Consent documents.
Clients Addressing The Adverse Events in Real Time
Adverse Events and Serious Adverse Events (AE/SAE) are critical for clinical trials and they can potentially shut down the trials if not handled properly. Many sites, especially in resource-poor settings, find it extremely difficult to adhere to the strict AE/SAE protocol requirements.
CliniOps provides trial administrators an ability to receive notification of an AE/SAE event in real-time from any of the trial sites across the world. One of our clients was exhilarated to see this innovation in action, which helped them respond to the situation in a timely manner with real-time access to AE/SAE reporting across all their sites’.
Awards & Recognition 2016
CliniOps Received 2016 Best of Fremont Award
CliniOps has been selected for the 2016 Best of Fremont Award in the Software Company category by the Fremont Award Program.
Scope Summit 2016
CliniOps CEO hosted an interactive Breakout discussion on ‘Leverage eSource and Mobile technology innovations, to conduct global clinical trials!!’ at the annual Scope Summit, Miami, FL, February 23, 2016.