Pre-clinical Data Services

The journey from preclinical development to first-in-human trials is all about doing the right things at the right time. A smart, data-driven strategy enhances your chances of success, optimizes efficacy and safety outcomes, and reduces the risk of suboptimal formulations or study results.

We empower you to optimize preclinical strategies using AI, advanced analytics, and digital tools, streamlining study planning, accelerating decision-making, and enabling evidence-based choices. Whether facing complex protocols or tight timelines, we provide tailored, technology-driven solutions that address your unique challenges—helping you accelerate development, enhance outcomes, and unlock the full potential of your portfolio.

Our preclinical experts can:

• Design and optimize preclinical study packages
• Monitor toxicity and safety pharmacology studies using digital data capture and AI-assisted analysis
• Evaluate results and integrate insights into regulatory documents and risk assessments
• Support end-to-end development planning, from early-stage studies to marketing approval and post-market activities

By combining expert guidance with AI-enabled tools, we help you navigate the complexities of drug development efficiently, make informed decisions faster, and capitalize on opportunities for success in an evolving regulatory and scientific landscape.