Decentralized Clinical Trials

Mainstream, Large Scale, Hybrid Trials

CliniOps Inc. is a Data Science company for the Life Science industry, to support digital Clinical trials, leveraging AI, mobile, analytics, cloud, sensors & connected devices. CliniOps's innovative mobile eClinical solutions, helps Pharma, Biotech & Medical device companies bring drugs & devices faster to market, with high data quality and less cost. CliniOps has a big focus on real-time decision support systems leveraging AI, ML & NLP, bringing a digital transformation in the life sciences industry.

Trials & Tribulations Post COVID-19

CliniOps Products

CliniOps offers a Unified Platform to support Hybrid and Virtual Clinical Trials, powered by Integrated Telemedicine. The solution is designed with study team stakeholders like you in mind, offering you the access to real-time data for informed decision making and seamless collaboration. The solution is structured to mimic the real world.

As with the demands of the growing clinical trials, your CliniOps platform has time and again proven to be extremely configurable and scalable, to meet your demands of the trials spanning several therapeutic areas, and the journey through your regulatory pathways across phase I, II, III & IV trials.

Study Portal

The Study Portal is a single unified platform to streamline ‘Clinical data management’, ‘Clinical operations’, and accelerated ‘Regulatory submission’ processes... Read more

Site App

The Site App is purpose-built mobile application that helps with the high quality & real-time electronic data collection at source (eSource). The application runs on standard... Read more

Patient App

The Patient App makes the clinical trials more Patient Centric by enabling data collection via telemedicine, with patients at their homes or at their normal care facility. It also... Read more

Our Services

CliniOps offers comprehensive data services to augment your in-house team, or the services provided by your CRO partner, throughout study startup, study conduct and study closeout phases. During study startup, our experienced configuration team supports the study build including configuration of forms, edit checks, workflows, reports, notifications et al., across all modules. A complete validation is also performed with CRF completion guidelines and release notes. During the study conduct phase, clinical data management, query resolution, user management and standard support services are provided. In addition, data reconciliation, DB lock, data transfer, data archival and other services are provided during the study closeout phase. Post that, CliniOps also provides, Biostatistics, TLF programming, ADaM, SDTM, and medical writing services.