Companies in biotech and pharma are spending a lot of time and effort in generating reports that must be validated. E.g., Continuous Process Verification (CPV), Impurity Profile Reports, Trend Reports, Stability Studies, Annual Product Reviews (APR), Product Quality Reviews (PQR), Release Reports.

In this webinar we show how to digitalize these efforts with a workflow-based approach. Our speciality is to access and prepare data. We add the necessary analytics and can produce tables, graphs that can be used in combination with reporting-templates, e.g., MS-Word and/or PDF.