ThoughtSphere is a software product company that focuses on enhancing the efficiency and effectiveness of processes in the pharma, life science and healthcare industries.

Our market-leading technologies help pharmaceutical, biopharma, medical device companies and CROs to reduce development costs and better identify risks when managing clinical trials.

If you are looking for better control of your clinical trials, near real-time overview, better quality data, more transparent and holistic risk management, and the flexibility to integrate different data sets and formats, you need to speak to us!

Company Overview

ThoughtSphere was founded by clinical information and technology industry experts with over 30 years of experience from the leading global CRO and eClinical providers. Our mission is to streamline and empower the clinical trials process by eliminating the two biggest challenges: integration of disparate clinical and operational data and making that data accessible for use with existing tools for analytics and visualizations. With ThoughtSphere’s innovative platform, pharma and biopharma companies, medical device sponsors and CROs can:

  • Reduce and optimize clinical development costs
  • Aggregate operational and clinical data to enhance efficiency and effectiveness in the clinical trial processes
  • Gain near real-time actionable insights for more effective RBM.

The product range includes our ClinACT clinical analytics and Risk-Based Monitoring solution, ClinDAP data aggregation platform and SPACE site payment and contracting environment. We have built the only clinical trial data platform that ensures patient safety, maintains regulatory compliance and controls trial costs in a uniquely integrated way.

Our new data management tool, DMSphere, and our new Business Intelligence (BI) Tool allow for enhanced trial oversight through faster, cleaner data and revolutionary data visualization and analysis.

Contact us to find out more about how our innovative solutions can help improve the effectiveness of your clinical trials.