My bookmarksSign up free

Commission Implementing Regulation (EU) 2025/2091 Article 10

Commission Implementing Regulation (EU) 2025/2091 Article 10

Training

Article 10

1.   All personnel shall receive initial and continuous training relevant to the tasks assigned. Training on the pharmaceutical quality system and good manufacturing practice shall be provided for personnel whose duties take them into production and storage areas or into control laboratories, and for other personnel whose activities may have an impact on the quality of the product. Personnel working in areas where contamination is a hazard, such as clean areas or areas where highly active, toxic, infectious or sensitising materials are handled, shall be given specific training. Training shall also include the hygiene programmes referred to in Article 11. 2.   The practical effectiveness of training shall be periodically assessed. Records of the trainings shall be kept.

Read the full instrument → · Read this in context: CHAPTER III — PERSONNEL →

Other provisions in CHAPTER III — PERSONNEL

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 10 of Commission Implementing Regulation (EU) 2025/2091 (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.

What to look at next