Many Quality Control (QC) laboratories in pharma- and biomanufacturing have not yet achieved digital transformation yet. In fact, many are still using paper and basic generic tools. This leads to cumbersome and time-consuming quality testing. Sampling and test execution, data entry and review, reporting and documentation, approval and certification—QC Labs need to accomplish all these steps according to defined procedures and in compliance with regulations. It is impossible to do so efficiently without a true digital system.
True digitalization—connecting people, processes, and data together—is the best way to improve productivity and enhance regulatory compliance. Open, platform-based solutions enable standardization, data aggregation through common models, and integrated analytics and visualizations. In this webinar our panel of experts will articulate a realistic and achievable vision for QC labs that will help increase productivity for timely batch release while improving data integrity and regulatory compliance.