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This on-demand webinar features presenters Bob McDowall and Christoph Jansen. Learn how regulatory pressure is pushing pharmaceutical companies to transition quality control from paper to electronic records. This process requires Computerized System Validation (CSV), which can appear extremely complex and time-consuming.
This webinar guides you through the process of Computerized System Validation in line with regulatory requirements. You will also learn about important milestones and estimated implementation times, as well as possible pitfalls. General recommendations for speedy and cost-effective processes are also included in the presentation.
QA/QC managers and IT project managers who have to perform a CSV.