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Commission Implementing Regulation (EU) No 520/2012 Article 13

Commission Implementing Regulation (EU) No 520/2012 Article 13

Audit

Article 13

1.   Risk-based audits of the quality system shall be performed at regular intervals to ensure that the quality system complies with the quality system requirements set out in Articles 8, 10, 11 and 12 and to determine its effectiveness. Those audits shall be conducted by individuals who have no direct involvement in or responsibility for the matters or processes being audited. 2.   Corrective action(s), including a follow-up audit of deficiencies, shall be taken where necessary. A report on the results of the audit shall be drawn up for each audit and follow-up audit. The audit report shall be sent to the management responsible for the matters audited. The dates and results of audits and follow-up audits shall be documented in accordance with the second subparagraph of Article 104(2) of Directive 2001/83/EC.

Read the full instrument → · Read this in context: Section 2 — Minimum requirements for the quality systems for the performance of pharmacovigilance activities by marketing authorisation holders →

Other provisions in Section 2 — Minimum requirements for the quality systems for the performance of pharmacovigilance activities by marketing authorisation holders

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 13 of Commission Implementing Regulation (EU) No 520/2012 (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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