Drive Data Integrity And Compliance In Bioanalysis Through Digital Transformation
Bioanalysis groups can quickly realize critical milestones by eliminating redundant processes, streamlining efficiency and optimizing workflows – important measures of preclinical/clinical success.
While advances in detection techniques and instrumentation have vastly improved, novel approaches are required in driving efficiency and data integrity for the myriad of processes that drive sample analysis through successful digital transformation.
Learn how a combination of controlled compliant workflow execution, dramatically streamlined data acquisition and an “audit by exception” approach offers the next phase of innovation within bioanalysis.
Speaker Ajaz Rosul, Lead Solutions Consultant for IDBS, breaks down the following topics:
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Why adding more resources is not the answer to capacity issues
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What your LIMS may not be telling you
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How to drive data integrity and efficiency to increase sample throughput
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How real-time QC can significantly reduce study cycle times
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How you can de-risk audits with traceable reporting at your fingertips
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How digital transformation can ensure compliance to build credibility and control operating costs
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