Instem is pleased to participate in PharmaTech Expo 2026, taking place in Gandhinagar, Gujarat.
Visit the Instem team at booth E94 to learn how our innovative software solutions support research, development, regulatory compliance, and data-driven decision-making across the product development lifecycle.
We look forward to connecting with customers, partners, and industry professionals throughout the event.
Streamlines end-to-end workflows for preclinical study management. Ask about our new Non-GLP Pathology module!
An advanced In Silico toxicology tool that helps scientists predict toxicity endpoints, review results with confidence, and generate regulatory-compliant reports. Ask the team for a demo of our new Toxicity Profiler!
Our Predict service uses advanced QSAR techniques to streamline early-stage safety assessments through predictive modeling. Enables researchers to evaluate potential toxicity risks quickly, supporting data-driven decision-making and reducing the need for subject testing.
Discovery solution optimizing bioanalysis workflows, accelerating in vitro ADME/DMPK studies and in vivo PK studies.
Simplifies the process of capturing, analyzing, and reporting data for faster discovery research.
Configurable LIMS covering data collection, storage, and reporting while meeting global compliance and quality standards.
Audit trail and data integrity solution for scientific systems and files.
Quality System Management (eQCM)NEW
Electronic quality management system for regulatory compliance processes.
An electronic laboratory notebook (ELN) that simplifies and streamlines the digitization and documentation of lab processes.
SEND Advantage™ Outsourced Services and Consulting
A suite of services that ensure your nonclinical data meets the Standard for Exchange of Nonclinical Data (SEND) submission requirements.
Submit™ Seamless Electronic SEND Submissions
A suite of services that ensure your nonclinical data meets the Standard for Exchange of Nonclinical Data (SEND) submission requirements.
Enables improved management of genotoxicity studies, delivering enhanced accuracy, documentation and compliance.
Want to talk in more detail? Contact us to schedule a 1:1 meeting. We look forward to seeing you there!
For more information, visit the Event Website
