Clinevo Technologies AI-Driven Software Solutions for Life Sciences R&D

What is Clinevo Technologies?

Clinevo Technologies is a specialized software development company focused on creating and implementing robust technology solutions tailored for Life Sciences R&D. They assist pharmaceutical companies, biotechnology firms, and Contract Research Organizations (CROs) in optimizing clinical trial processes by leveraging innovative technologies such as Data Warehousing, Analytics, Automation, and Artificial Intelligence. Their primary goal is to reduce the time and costs associated with clinical trials while ensuring efficiency and practicality.

The company emphasizes delivering end-to-end solutions that adhere to stringent regulatory guidelines, including HIPAA, GXP, CSV, and 21 CFR Part 11. Clinevo's extensive domain experience combined with technology expertise allows them to provide highly effective software for clinical trials, data warehousing, drug safety, and electronic trial master file (eTMF) management, serving clients globally across India, the USA, and Europe.

Features

Integrated Digital Clinical Trial Platform: Enables collaborative management of all clinical trial aspects.
Clinical Trial Management System (CTMS): End-to-end platform for managing clinical trials.
Electronic Trial Master File (eTMF): Organizes and stores digital clinical trial documents.
Electronic Data Capture (EDC) / eCRF: System for electronic capture of clinical trial data.
Pharmacovigilance Database: End-to-end drug safety system including PV Intake, Case Processing, Submissions, Analytics, and Signal Detection.
Remote Monitoring / rSDV / rSDR: Facilitates remote Source Data Verification and Review.
Master Data Management (MDM): Centralizes management of Sites, Investigators, and other trial information.
Clinical Data Warehouse & Automation: Consolidates and reports diverse clinical trial data.
AI-Enhanced Analytics & Automation: Utilizes AI for improved data insights and process automation.
Regulatory Compliance: Adheres to HIPAA, GXP, CSV, 21 CFR Part 11 guidelines.

Use Cases

Managing end-to-end clinical trial operations.
Organizing and storing essential clinical trial documentation electronically.
Capturing and managing clinical trial data through electronic forms.
Conducting remote monitoring and source data verification for clinical trials.
Managing drug safety reporting and pharmacovigilance processes.
Centralizing and ensuring uniformity of master data (sites, investigators).
Consolidating, analyzing, and reporting diverse clinical trial data.
Automating repetitive tasks within clinical research and development.
Ensuring software solutions meet regulatory compliance standards in life sciences.