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Commission Delegated Regulation (EU) 2016/161 Article 11

Commission Delegated Regulation (EU) 2016/161 Article 11

Verification of the authenticity of the unique identifier

Article 11

When verifying the authenticity of a unique identifier, manufacturers, wholesalers and persons authorised or entitled to supply medicinal products to the public shall check the unique identifier against the unique identifiers stored in the repositories system referred to in Article 31. A unique identifier shall be considered authentic when the repositories system contains an active unique identifier with the product code and serial number that are identical to those of the unique identifier being verified.

Read the full instrument → · Read this in context: CHAPTER III — GENERAL PROVISIONS ON THE VERIFICATION OF THE SAFETY FEATURES →

Other provisions in CHAPTER III — GENERAL PROVISIONS ON THE VERIFICATION OF THE SAFETY FEATURES

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 11 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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