ClinTop Edge
Clinical Technologies
Smart Tools for Smarter Trials
MedInventas offers proprietary eClinical solutions designed to simplify and optimize trial execution. Our platforms integrate seamlessly to provide sponsors and CRO partners with real-time insights, risk mitigation, and streamlined workflows.
MedInventas also offers individual technology modules to cater to the needs of the clients
ClinTop Edge : Clinical Operations Technology
ClinTop Design
Protocol Synopsis Drafting Tool
AI-powered structured authoring for protocol synopsis & optimisation. Saves 30% – 40% protocol development time
ClinTop Assess
Feasibility & Site Selection Tool.
For efficient study and site feasibility. Sending feasibility questionnaire & getting response, analyzing data and ranking sites based on feasibility response
ClinTop Engage
Site Communication & Document Exchange Platform
For site communication and document exchange between sites and sponsor/CRO. EC submission & important document distribution & tracking
ClinTop Assign
RTSM (Randomization & Trial Supply Management)
Randomization and study Supply Management system. Flexible randomization strategies, realtime drug accountability shipment tracking & predictive supply algorithm to minimize wastage
ClinTop Capture
EDC (Electronic Data Capture)
Electronic Data Capture and Data management tool. Intuitive, parameter driven eCRF design with drag-and-drop builder. Real-time data validation & edit checks. 21 CFR Part 11 compliant audit trails
ClinTop Monitor
CTMS with RBM (Risk-Based Monitoring)
For reports related to clinical trial operations, site metrics. For risk based monitoring and centralized monitoring (CTMS + Centralized Monitoring)
Benefits of ClinTop Edge Technology
- End-to-end platform: fully modular or integrated
- Flexibility to offer individual modules based on clients’ needs
- Built with compliance, scalability, and user experience at core
- Faster deployment → reduced study startup times
- Real-time visibility and analytics
- Audit readiness
- Improved collaboration between sponsors, CROs, and sites
Site Edge is the platform built for investigational study sites to identify, engage and manage their patients on clinical trial efficiently.
Site Edge : For Investigational Site Operations
Patient Screener
For identifying and filtering potential patients from sites EHR data base as the clinical trial protocol criteria. Reduces the patient identification time significantly. Only investigators/ sites will have access to this tool
Patient Tracker
Potential patients will be tracked after identifying till the patient is enrolled in the clinical study. This include sending study details to the patients, sending ICF to the interested patients till patient get randomized
Site Support
This will help investigators and site staff to get responses to their questions on study, protocol IB & ICFs. Realtime support to answer site’s queries instead of waiting for CRA or medical monitor response
e-Consent
An innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials. It also enhances the patient experience with easy-to-understand clinical trial information, patient compliance and boosting patient engagement.
