To bring new therapies to the patients faster, we need to bring people, processes and data together across the full pharma process development lifecycle.
Transferring product, process and equipment knowledge between R&D and manufacturing teams is complex, expensive and time-consuming.
Making data a core deliverable means the right people need to collect information and connect disparate data points through a well-structured data backbone.
In this webinar, we share how a combination of controlled compliant workflow execution, dramatically streamlined data acquisition and an “audit by exception” approach is the next phase of innovation within bioanalysis.
Explore why digital maturity is key to transparency and collaboration and enabling accurate forecasting throughout the BioPharmaceutical lifecycle.