Overview
STARLIMS provides a comprehensive Laboratory Information Management System (LIMS) tailored for pharmaceutical, biotechnology, and CDMO labs, integrating ELN, SDMS, LES, and analytics for workflow automation, sample tracking, and data management. The platform ensures regulatory compliance with standards like FDA 21 CFR Part 11, EU Annex 11, ISO 17025, and cGXP, while optimizing lab efficiency and reducing costs. With over 35 years of experience, STARLIMS serves global customers across more than 40 countries.
Frequently asked questions
- What core capabilities does STARLIMS offer for pharma labs?
- STARLIMS delivers LIMS with sample lifecycle management, workflow automation, batch release, quality control, instrument integration, electronic signatures, audit trails, and advanced analytics for operational efficiency.
- Which regulatory standards does STARLIMS support?
- STARLIMS complies with FDA 21 CFR Part 11, EU Annex 11, ISO 17025, ISO 9001:2015, ISO 27001:2022, cGXP, ASCLD-LAB, and CALEA, ensuring data integrity across diverse environments.
- What industries and geographies does STARLIMS serve?
- STARLIMS supports pharmaceutical, biotech, CDMO, clinical diagnostics, and other sectors, with deployments in over 40 countries via 12 global development and support centers.