Interviews, Smart Manufacturing

Challenges and necessities for SecurPharm

Thomas Brückner, Head of Pharmaceutical Affairs, GMP, Medical Devices of the German Pharmaceutical Industry Association e.V., explained incoming regulation changes for Pharma companies. Due to the new delegated regulation on safety features for medicinal products adopted by the European Commission, new challenges and necessities for the pharmaceutical manufacturers arise. Mr. Brückner states that Serialization and verification on single pack level are main aspects of the new regulation. He also mentioned the requirements to join secur-Pharm, Europe‘s first stakeholder-driven verification system for medicinal products.

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