Commission Implementing Regulation (EU) No 520/2012 Article 29

Format of electronic transmission of suspected adverse reactions

Article 29

Member States and marketing authorisation holders shall use the formats provided for in Article 26 and the terminology provided for in Article 25 for the electronic transmission of suspected adverse reactions.

Read the full instrument → · Read this in context: CHAPTER V — Transmission of reports of suspected adverse reactions →

Other provisions in CHAPTER V — Transmission of reports of suspected adverse reactions

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 29 of Commission Implementing Regulation (EU) No 520/2012 (LawPlayer, data as of 2026-07-04)

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