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Commission Delegated Regulation (EU) 2016/161 Article 47

Evaluation of the notifications

Article 47

Where, following a notification as referred to in Article 46, the Commission or a Member State considers, on the basis of casualties or hospitalisations of citizens of the Union due to exposure to falsified medicinal products, that rapid action is required to protect public health, the Commission shall asses the notification without delay and at the latest within 45 days.

Read the full instrument → · Read this in context: CHAPTER X — LISTS OF DEROGATIONS AND NOTIFICATIONS TO THE COMMISSION →

Other provisions in CHAPTER X — LISTS OF DEROGATIONS AND NOTIFICATIONS TO THE COMMISSION

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationArticle 47 of Commission Delegated Regulation (EU) 2016/161 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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