Commission Delegated Regulation (EU) 2017/1569 Article 15

Self-inspection by the manufacturer

Article 15

The manufacturer shall conduct regular inspections as part of the pharmaceutical quality system in order to monitor the implementation and respect of good manufacturing practice. He shall take any necessary corrective action and to put in place any necessary preventive measures. The manufacturer shall maintain records of all such inspections and any corrective action or preventive measures subsequently taken.

Read the full instrument → · Read this in context: CHAPTER II — GOOD MANUFACTURING PRACTICE →

Other provisions in CHAPTER II — GOOD MANUFACTURING 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 15 of Commission Delegated Regulation (EU) 2017/1569 (LawPlayer, data as of 2026-07-04)

What to look at next

Commission Delegated Regulation (EU) 2017/1569, full textChapter navigation and full text, so you can read this section in contextEuropean Union legislation EU Legal Acts by type and yearGrouped by instrument type and year of enactment, so you can find others of the same kindBrowse by type and year CHAPTER II — GOOD MANUFACTURING PRACTICE — read this in contextThe surrounding text of the act in order, so you can see what comes before and afterChapters and sections