Reducing bottlenecks in GMP Laboratories
Significant time is spent conducting quality control (QC) testing and documenting QC results during the pharmaceutical manufacturing process. GMP regulations require maintaining documentation to ensure strict compliance with established SOP’s. Completing paper documents and ensuring their authenticity creates a bottleneck in the QC laboratory. Waters® NuGenesis® SDMS Intelligent Procedure Manager, an electronic SOP workflow & documentation system, addresses the predominately manual activities required to perform an analytical method. Cycle times are reduced up to 50-75% as compared to a traditional paper trail thereby boosting productivity and accuracy.
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Managed Innovation, Assured Compliance
Developing, executing and managing the transformation, analysis and submission of clinical research data with SAS® Drug Development
Get better products to market faster. Download this white paper to discover the top ten challenges facing life science executives and how to overcome them. See how SAS Drug Development transforms clinical data into true innovation.
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Coherent IT Strategy for Fast-Moving R&D;
Putting value on an IT strategy is easier with an end-to-end view, from target to market, of the cause and effect of good and bad information and decisions. This forges the essential link between science, information, IT and business funding of the IT investment. This paper seeks to:
- Help biopharm companies build effective IT for R&D; strategies.
- Deploy highly relevant systems around a particular set of goals.
- Discuss case studies where this approach has returned better business value.
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