How validation is easier for Galenica with Bizzmine

Audit Management CAPA Management Complaint Management Document Control Pharma

Galenica AB supports and guides our partners in their pharmaceutical development programs. We are experts at pharmaceutical and analytical development and production of Clinical Trial Material (CTM) for Phase I – III. Galenica AB also manufactures commercially niched products for the market. We need to comply with the pharmaceutical regulations of the European Union and are authorized and audited by the Swedish Medical Product Agency.

Creating and validating automated business processes have probably never been easier.