Companies in the pharmaceutical industry must gather data efficiently and reliably, while protecting their data with a secure and fully auditable system. A successful pharmaceutical LIMS implementation will also reduce costs, improve the quality of collected data, and reduce time to market for products.
The Core system manages all aspects of the testing, workflow, reporting, and regulatory requirements necessary in a pharmaceutical LIMS. Components for in-vitro studies are customized to fit with clients� workflows. Stability determination and dissolution testing can be handled through configuration of the Core LIMS. Advanced data tracking, such as for the chemical properties, formulation, excipients, etc. of a compound, is available because of the system�s flexibility in the definition of object attributes.
With the powerful analytical tools of the Core LIMS, companies can save time and money by identifying problems with new targets earlier in the drug discovery cycle. The system includes end-user driven data validation and curve-fitting capabilities to aid labs in the analysis of their data to determine whether a target is worth pursuing or not. By discovering bad candidates earlier, labs can save the money that would otherwise have been used on further research and testing with those targets; this money can instead be used to find new candidates.