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Council Regulation (EC) No 1186/2009 Article 55

Council Regulation (EC) No 1186/2009 Article 55

Article 55

Relief shall be limited to products which: (a) are intended for institutions or laboratories approved by the competent authorities, for use exclusively for non-commercial medical or scientific purposes; (b) are accompanied by a certificate of conformity issued by a duly authorised body in the third country of departure; (c) are in containers bearing a special label identifying them.

Read the full instrument → · Read this in context: CHAPTER XIII — Therapeutic substances of human origin and blood-grouping and tissue-typing reagents →

Other provisions in CHAPTER XIII — Therapeutic substances of human origin and blood-grouping and tissue-typing reagents

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 55 of Council Regulation (EC) No 1186/2009 (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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