Unified Trial Platform

With a vision of bringing Transparency, Data Integrity and Real-time Analysis to all Clinical Trials, ClinIV aims to transform and modernize the current methods of Clinical Trial Execution by bringing in Digitization & Mobility to
  • Bring in Rapid Operational Efficiencies
  • Ensure Quicker Time-to-Completion of Trials
  • Focus on Strict Process Compliance
  • Maintain High Ethical standards
  • Provide High Data Security and Integrity
To ensure quicker time to market for the Companies.
Easy Participant recruitment and Trial Findings
Digitized Case Report Forms (eCRFs)
Participant Consent Forms (e-Consent)
Comprehensive Protocol Creation tool
Remote Participant Monitoring, Follow-ups and Engagement
Detailed Electronic Health Records (EHR)
eReviews across the Hierarchy
Device Agnostic (Works on any device – Mobile/Web)
Real-time Dashboards, Reports & Analytics

The ClinIV Clinical Cloud, your platform of choice for clinical research.

The ClinIV Clinical Cloud™ is our cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, and research sites. Designed as a unified data platform, the ClinIV Clinical Cloud creates a single source of truth for all study-related data. Simply put, enter data once and let the platform master and populate it throughout the end-to-end suite of ClinIV applications.
Optimize operational execution, decrease the data entry and maintenance burden, and reduce the number of clinical systems across your study teams. Throw away your list of passwords and excel sheets, you are now on a truly unified platform.
ClinIV Clinical Cloud accelerates the business of clinical research with an end-to-end suite of CliniV applications for Data Capture, Data Management, Trial Planning, Trial Management, and Analytics powered by a rich set of Platform Tools.
The ClinIV Clinical Cloud unifies ClinIV’s end-to-end solutions that support the entire clinical trial process. Whether you’re working in Study Conduct, Study Management or both, our platform is the most powerful and comprehensive one in the industry.

Real World Evidence

Predictive Analysis of patient health outcome and performance of drugs
Automatic Generation & Risk assessment of Clinical Outcomes
Integration with tools for :
  • Scientific data modelling
  • Patient cohort management
  • Unstructured text analysis
  • Clinical data modelling
Real time monitoring of adverse events & SAE’s through Alerts & Notifications

Realtime Monitoring

Cliniv promotes a hurdle-free execution of Clinical Trials.

Cliniv allows a comprehensive oversight on the operations and execution of any phase of a Clinical Trial. It is a Site-agonistic tool, that caters to both on-site and off-site (remote) clinical trials.

It allows Trial Owners to digitize the screening and enrolment process and helps engage the participants early, reduce study timelines and minimize Participant Drop-outs. It also helps facilitate Participant engagement through remote and DIY tools such as – Participant Diaries, Tele-Consultation etc. Cliniv allows remote Consent, Screening and Enrollment of Subjects into the Trial.

Furthermore, through the use of effective Telemedicine in conjunction with integrated Approved Screening Devices, Subject Follow-ups and Monitoring becomes much easier – hence reducing the burden on the Participants and the Sites.

Cliniv effectively addresses the complexities involved in the execution of Clinical Trials which are traditionally burdened with, among other things, cumbersome paper-based processes, tedious subject recruitments and constant mid-trial subject drop-outs. Cliniv also facilitates remote Trial execution which significantly limits the need of Subjects’ physical presence at the Trial sites.