Kitsa, the AI operating system for clinical trial start-up, today announced a strategic partnership with Tech Mahindra, a leading global provider of technology consulting and digital solutions to enterprises across industries, to advance agentic AI–driven medical writing solutions for the global pharmaceutical and biotechnology industry. The partnership represents the latest in Kitsa’s growing network of global technology alliances, as the company scales its reach across the pharmaceutical value chain.
The partnership further strengthens Tech Mahindra’s Gen AI Medical Writing offering for Life Sciences by integrating Kitsa’s KScribe platform, enabling pharmaceutical sponsors and CROs to accelerate clinical trial protocol development and regulatory documentation using purpose-built artificial intelligence.
Through this partnership, Tech Mahindra will enhance the go-to-market capabilities to its global pharmaceutical and biotech customer base, helping organizations modernize clinical development workflows at scale.
Compressing Clinical Timelines: From Months to Days
Clinical trial protocols - the blueprints that define how a study is conducted - often require 8 to 12 weeks of manual coordination across clinical scientists, statisticians, regulatory experts, and medical writers. By combining Kitsa’s domain-specific AI models, structured protocol design frameworks, and historical trial intelligence, the joint solution enables clinical teams to draft high-quality protocols in days instead of months, while improving consistency and regulatory readiness.
Kitsa’s KScribe platform applies specialized AI trained on clinical trial protocols, regulatory guidance, and historical study data to assist medical writers and clinical teams with:
- Structured clinical trial protocol drafting and study design
- Regulatory-ready documentation aligned with global guidance frameworks
- Data-driven benchmarking of study designs against historical trial data
Executive Perspectives
“Clinical development is entering a new era where agentic AI systems augment scientific teams and dramatically accelerate the path from protocol design to first patient enrolled. This partnership with Tech Mahindra builds on our growing network of global alliances and reflects the momentum Kitsa has built as the AI operating system for clinical trial start-up. Together, we are enabling clinical teams worldwide to design and launch trials faster — while maintaining the rigor that regulators and sponsors demand.”
Ajay Nyamati, CEO and Co-Founder, Kitsa
“Medical writing and protocol development continue to be weighed down by fragmented workflows, intensive manual effort, and the growing complexity of global regulatory requirements. Our partnership with Kitsa addresses this challenge by combining Tech Mahindra’s GenAI-led Life Sciences capabilities with Kitsa’s purpose-built KScribe platform to help pharmaceutical and biotechnology organizations reimagine how protocols and regulatory documents are developed. Together, we are enabling faster, more consistent, and regulatory-ready medical writing workflows, helping organizations accelerate study start-up, improve operational efficiency, and bring greater agility.”
Ravinder Singh, Global Vertical Service Line Head – HLS, Tech Mahindra
Available on AWS Marketplace
The joint ‘Clinical Document Studio’ solution is available through the AWS Marketplace, enabling pharmaceutical organizations to rapidly deploy AI-driven protocol development and regulatory authoring capabilities. AWS Marketplace deployment means sponsors can procure and activate KScribe-powered workflows through existing AWS procurement channels, reducing friction, meeting enterprise security requirements, and accelerating time-to-value.
