Why choose STARLIMS:
1. The STARLIMS advanced analysis dashboard has a high degree of visualization to assist management in making informed decisions.
2. A unified platform can reduce the complexity of third-party integration, reduce total cost of ownership, and simplify integration verification
3. A platform provides a highly automated integrated solution that can bring better data integrity
4. Follow compliance requirements and regulatory processes and procedures in all workflows
5. A single system can be suitable for all business areas, including research and development, clinical trials, and manufacturing
Integrated solution: secure, reliable, and integrated
STARLIMS provides you with an integrated solution that integrates LIMS, ELN, SMDS, advanced analytics, and mobile applications into one application platform. As an industry leader, STARLIMS provides various functions to assist you in supervising and controlling the safety and quality of raw materials, intermediate products, and finished products; It provides you with a secure and reliable platform for result archiving and information management.
Pharmaceutical and Biotechnology Laboratory Management:
The STARLIMS laboratory information management system provides powerful tools to support comprehensive management of all laboratory processes:
1. Instrument management, inventory control, formula management
2. Flexible computing, reporting, and data analysis tools
3. Analysis batch and enzyme label management
4. Standard reagent management
5. Comprehensive audit trail and electronic signature
6. Stability research and microbial management
7. Schedule and Capacity Planning
8. Chromatographic data system (CDS) integration, etc
Improving regulatory compliance:
STARLIMS pharmaceutical and biotechnology solutions have rich cases in the pharmaceutical, medical equipment, contract laboratories, and biotechnology industries. It is an extended web-based product that allows you to use features that fully comply with 21 CFR Part 11 specifications anytime, anywhere to ensure data integrity, regulatory compliance, and ready for inspection at any time
1. Integrate sample data and documents
2. Victory analysis certificate for samples that meet specifications
3. Generate stability research summary report
4. Analyze trends and handle ICH, USP, JP, and EP testing standards
5. Comply with cGxP, FDA, ANVISA, ISO17025, and other regulatory requirements and best practices
6. Real time analysis of generated test samples
