Overview:
Founded in 2016, we are an IT Services and Software Development Company specialized in developing and implementing robust technology solutions for Life Sciences domain. We help Pharma, Biotech and CROs in reducing their time and cost in Clinical trials by implementing innovative technologies that  Data warehousing, Analytics, Collaboration, Automation, and Artificial Intelligence.

With our unmatched combination of domain experience & technology expertise, we are committed to delivering the most efficient and practical end-to-end solutions with HIPAA, GXP, CSV, 21 CFR Part 11 and other applicable regulatory guidelines. Our unmatched domain experience and technology to deliver best solutions.

Vision:
Our vision is to Improve Healthcare by Reducing Time and Cost of Clinical Trials by developing and implementing innovative technologies.

Mission:
Develop and Implement an integrated platform for Life Sciences Industry that enables data warehousing, Analytics, Collaboration, Automation and AI across the clinical research enterprise.

Our Products:

Safety: 
Clinevo OnePharmacovigilance
Clinevo Safety (PV Database)
MICC Intake
Website Intake
Signal Detection
Safety Analytics

Clinical: 
Clinevo One Clinical Trial Platform
Clinical Trial Mamanegement System (CTMS)
Electronic Trial Master File (eTMF)
Remote Source Data Verification (r-SDV) / Remote Monitoring
Electronic Investigator Site Files (eISF)
Electronic Data Capture (EDC)/ eCRF
Master Data Management (MDM)
Meta Data Repository (MDR)

Quality:
Clinevo One Quality Management System (OneQMS)
Document Management System (DMS)
Training Management System/ Learning Management (eLearn)

Datawarehouse:
Clinical Data Warehouse & Automation Console



Biotechnology

Clinical Trials

Life Sciences

Pharmaceutical

Clinevo Technologies

Clinevo Technologies' headquarters in Bangalore, India

Mani Vasudevan

Santhosh Kumar

Madhu Varma

The Project Management team at Clinevo Technologies is responsible for the planning, execution, and delivery of technology solutions tailored for the Life Sciences domain. They coordinate with various stakeholders, including account managers, directors, consultants, and QA teams, to streamline clinical trial processes through the implementation of data warehousing, analytics, collaboration, automation, and AI. The team ensures that all projects adhere to regulatory guidelines such as HIPAA, GXP, CSV, and 21 CFR Part 11 while focusing on reducing the time and cost of clinical trials.

Project Management

The Software Development team at Clinevo Technologies is responsible for designing, developing, and implementing cutting-edge software solutions tailored for the Life Sciences domain. This team collaborates closely to create and enhance products such as the Clinevo OnePharmacovigilance, Clinical Trial Management System (CTMS), and the Clinevo One Quality Management System (OneQMS). They ensure compliance with regulatory guidelines including HIPAA, GXP, and 21 CFR Part 11 while integrating advanced technologies like data warehousing, analytics, automation, and artificial intelligence to improve clinical trial efficiency and reduce costs.

Clinevo Technologies

Org chart

Teams

Project Management

Software Development

Offices

Clinevo Technologies

Org chart

Teams

Project Management

Software Development

Offices

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