by Instem Team | Jul 16, 2025 | Resources
Health Agencies like Health Canada have been raising the standards and requirements for sharing clinical trial data. This increasing pressure on life science companies to share Clinical Study Reports (CSRs) has put a strain on Clinical Transparency teams. Download...
by Instem Team | Jul 16, 2025 | Resources
To unify workflows, reduce manual effort, and ensure GLP compliance, a leading European pharmaceutical company implemented Instem’s Cyto Study Manager™ in its genetic toxicology research. Seamlessly integrating with their existing Metafer4/Relosys4 image analysis...
by Instem Team | Jul 16, 2025 | Resources
Cyto Study Manager™ is a powerful, GLP-compliant platform that centralizes and simplifies genetic toxicology workflows. With modular design, customizable templates, and seamless integration across assay types, it reduces manual effort, eliminates transcription errors,...
by Instem Team | Jul 11, 2025 | Clinical
Clinical trials are growing in complexity, due to higher data volumes, more diverse data types, greater international collaboration, and shifting regulatory demands. These developments place increasing pressure on data analysis teams who must integrate and analyze...
by Instem Team | Jul 7, 2025 | Clinical
The life sciences industry is producing more data than ever before. Global clinical trials operations and analytics now span multiple geographies, data sources, and regulatory requirements. As a result, legacy systems can no longer keep pace with the demands of...
