CPHI Milan newsletter
PCI High Potent Manufacturing
LB Bohle – 10.06.2025
Temax_Krautz

Current Edition

Current Edition

CDMO Subsection

Insights into the latest developments in CDMO services and manufacturing.

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Injectables Subsection

Expert perspectives on the evolving needs of injectable therapies and packaging.

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Nasal & Pulmonary Subsection

Exploring the latest developments in inhalation technologies, respiratory delivery and sustainability

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CPHI Milan
DDL 2026

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Nipro August 26

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Merxin March 2026

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Lifecore Biomedical

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Solstice

EU Falsified Medicines Directive (FMD) – A Technical & Implementation Success

Since early 2019, manufacturers of pharmaceutical goods have been required to add additional security labelling to certain products sold in the European Union. Under the terms of the EU Falsified Medicines Directive (EU FMD), prescription pharmaceutical products are now required to have a verifiable 2D data matrix code and tamper-evident labelling included as part of their product packaging. In addition, Bart
Vansteenkiste at Domino Printing Sciences clarifies that a humanreadable unique serial number is required to meet the Directive’s requirements, as well as a product code, batch number, and expiry date for the contents.

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MedPharm 16/07

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Biopharma group march 2026

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Silgan March 2026

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Terumo 06/26

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Scott Pharma – 25.03.2025

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Bespak

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Tjoapack
Aptar – 08/01/2026