Contract
serialization
As of February 9, 2019, the provisions of Commission Delegated Regulation (EU) 2016/161 regarding safety features for medicinal products became applicable in Poland, mandating that manufacturers implement specific security measures. This presented a significant challenge for pharmaceutical manufacturers and contract manufacturers, requiring them to adapt their production processes, as well as their technical and IT infrastructure, to the standards defined in the regulation.
Contract serialization of medicinal products
We provide contract serialization for medicinal products and products containing controlled substances, including those requiring cold chain storage (+2°C to +8°C). Our services are delivered as part of an integrated project covering production, serialization data management, data communication to and from the client, as well as decommissioning (deserialization).
This ensures full product identification throughout the distribution chain and protects the product against falsification.
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