The European Commission has published Q&A regarding the safety features of medicinal products

The European Commission has published on its website a list of questions and answers regarding obligation of safety features appearing on the packaging of medicinal products for human use. As it is well known, from February 9, 2019, entrepreneurs will be required to put on the packaging of medicinal products an unique identifier and an anti-tampering device (so-called “safety features”).

We encourage you to read the full overview at: https://ec.europa.eu/health/sites/health/files/files/falsified_medicines/qa_safetyfeature_en.pdf