Automated Efficiency in Pharmaceutical Documentation
Quantifiable Impact:
- 30% time-saving in regulatory documentation preparation
- $5M cost-saving in specialised staff costs
In the highly-regulated pharmaceutical landscape, bringing a new drug to market involves navigating complex documentation processes, governed by stringent entities like the FDA and EMA. Our client, a leading pharmaceutical entity, faced prolonged data synthesis timelines, manual-input errors, and disparate data systems.
Goals
In collaboration with our client, we outlined key project objectives:
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Operational Efficiency: dramatically reduce the time needed for generating the data visualisation like tables and charts
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Data Accuracy: substantially reduce data errors, especially those arising from manual inputs
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Data Consolidation: seamlessly unify fragmented data sources to foster a consistent, comprehensive data environment
Our Solutions
Sentium’s bespoke approach addressed the unique challenges of pharmaceutical regulatory compliance:
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Unified Data Platform: integrated data sets ranging from manufacturing metrics to regulatory compliance measures into one robust platform
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Automated Visual Tools: implemented tools for the automatic generation of essential visual insights, built on a unified data foundation
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Optimised Workflows: integrated advanced workflow solutions to enhance data compliance and accessibility
Impact
Our solutions catalysed transformative changes:
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Time Efficiency: reduced chart and table generation time from days to... minutes!
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Document Turnaround: cut down regulatory document preparation time by 30%
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Cost Savings: yielded financial efficiencies, saving the client over $5 million in specialised staff costs