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Pharma and Biotechnology
QC/QA laboratories in the pharmaceutical industry have their own regulatory requirements to meet (GxP, 21CFR Part11). In addition to this the management of stability studies is often a major objective for their LIMS. For pharmaceutical and biotechnical research and development laboratories in drug discovery and high throughput screening, the requirements on the information management systems are often focusing on flexibility and configurability as the projects, experiments and methods used vary over time. Integration with scientific software packages is requested. LabVantage Sapphire LIMS meets all the above requirements.
Selected references
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| Finnish Red Cross Blood Transfusion Services, Finland |
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| National Bureau of Investigations (KRP), Finland |
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