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Regulation (EU) 2017/625 (OCR) Article 39

Regulation (EU) 2017/625 (OCR) Article 39

Audits of official laboratories

Article 39

1.   The competent authorities shall organise audits of the official laboratories they have designated in accordance with Article 37(1) on a regular basis and any time they consider that an audit is necessary, unless they find such audits to be redundant considering the accreditation assessment referred to in point (e) of Article 37(4). 2.   The competent authorities shall immediately withdraw the designation of an official laboratory, either completely or for certain tasks, where it fails to take appropriate and timely remedial action following the results of an audit provided for in paragraph 1 which disclose any of the following: (a) it no longer complies with the conditions provided for in Article 37(4) and (5); (b) it does not comply with the obligations provided for in Article 38; (c) it is underperforming at inter-laboratory comparative tests referred to in Article 38(2).

Read the full instrument → · Read this in context: CHAPTER IV — Sampling, analyses, tests and diagnoses →

Other provisions in CHAPTER IV — Sampling, analyses, tests and diagnoses

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 39 of Regulation (EU) 2017/625 (OCR) (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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