In the pharmaceutical industry, there is an ever-increasing need to quickly analyze incoming raw materials where both identification and purity results are critical. The accurate analysis of intermediates and final products is essential and compliance with FDA and GMP guidelines must be clearly documented.

• Chromatography
• Mass Spectrometry
• LIMS and CDS
• Laboratory Automation
• Materials Characterization and Pharmaceutical 
  Extrusion
• Process Instruments

Darwin LIMS meets the needs of pharmaceutical manufacturing R&D and QA/QC by providing application-specific functionality out of the box. The benefits are obvious: less customization means dramatically reduced implementation, training, validation and maintenance costs – for a lower total cost of ownership and high end-user acceptance.       More...

EP Series is a solution for the centralized GLP-compliant management, analysis, simulation and reporting of PK/PD laboratory data in drug development and provides LIMS capability for PK/PD laboratory data. Fully Integrated with the Kinetica data analysis and reporting tool, this solution provides enterprise-wide knowledge management. More...