Resources
Explore our Resource Hub: On-Demand Webinars, Brochures, Case Studies, and Insights to Accelerate Your Research.
Resource Type
Fact Sheet: Climb
Streamline Non-GLP In Vivo Study Management with Climb, a modern, cloud-based platform for efficient, compliant, and flexible preclinical research.
Fact Sheet: eQCM – The All-In-One Digital Quality Management System
eQCM empowers your business to stay compliant, reduce risks, and boost efficiency with a flexible cloud-based solution that adapts to your unique quality and regulatory needs.
Fact Sheet: Pristima – Unified Solution for the Preclinical Laboratory
Pristima provides a unified, intuitive platform for preclinical research management, streamlining workflows and empowering smarter, faster decisions with its comprehensive capabilities.
Matrix Gemini LIMS Fact Sheet
Matrix Gemini LIMS delivers a flexible, configurable, and future-proof solution for laboratories of all sizes, helping users manage samples, data, and workflows efficiently while ensuring full regulatory compliance.
Fact Sheet: SENDView™: Simplified Data Review
The SENDView solution is an easy-to-install/access product allowing clients rapid deployment after placing their activation order.
Fact Sheet: GuidePro™: Study Data Reviewer’s Guide Generator
GuidePro™, Instem’s nonclinical Study Data Reviewer’s Guide (nSDRG) generator, allows CROs, Sponsors and SEND creators to produce nSDRGs quickly and easily.
Fact Sheet: DefineNow™: Seamless define.xml File Creator and Editor
DefineNow™, Instem’s define.xml editor, lets CROs, Sponsors, and SEND creators quickly create and edit define files.
Fact Sheet: Cyto Study Manager™: Centralized Genotoxicity Data – Compliant, Reproducible, and Efficient
Cyto Study Manager™ supports diverse in vivo and in vitro assays, maintains GLP and 21 CFR Part 11 compliance, and generates complete, auditable data for regulatory submission.
Fact Sheet: Blur™: Simplifying and Streamlining Clinical Trial Transparency Compliance
Built by Pharma for Pharma, Blur is the Best-In-Class SaaS Solution for De-Identification of Clinical Trial Data, Safeguarding Patient Privacy, and Ensuring Regulatory Compliance.
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