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Commission Directive 2005/28/EC of 8 April 2005 laying down… Article 5

Commission Directive 2005/28/EC of 8 April 2005 laying down… Article 5

Article 5

All clinical trial information shall be recorded, handled, and stored in such a way that it can be accurately reported, interpreted and verified, while the confidentiality of records of the trial subjects remains protected.

Read the full instrument → · Read this in context: SECTION 1 — GOOD CLINICAL PRACTICE →

Other provisions in SECTION 1 — GOOD CLINICAL PRACTICE

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 5 of Commission Directive 2005/28/EC of 8 April 2005 laying down… (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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