Digitalize Validated Reporting in Pharma and Biotech

Thursday, February 24, 2022 – 16.00-17.15 CET


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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.

At the end, the whole process is automated, paperless and the creation of the reports takes only a fraction of the time it used to. Reports consisting of up to hundreds of pages are created in minutes.

In this webinar we show how we approach these challenges with our knowhow and solutions based on experience from many projects.


  • Introduction to the topic
  • User View - Validated Reporting as a service!
  • Solution View - How to get there – A process approach.
  • System Architecture View – Flexibility makes the difference and reduces costs.
  • Q & A and Summary


Michael Busch
Lead Data Engineer

Sören Schönfeld
Lead Data Engineer


Cosimo Caforio
Data Innovation & Life Sciences