What changed in GMP, and what does it touch?
Two questions matter when a requirement moves: what actually changed, and which of your processes now need review. This section answers the first from the authority's own text, and structures the second.
No regulatory development is inferred, predicted or reconstructed from memory. Entries appear only when verified against the issuing authority, and each says so.
Calendar last reviewed 2026-09-05. Currently 4 verified entries.
Track, analyse, verify
Regulatory calendar
Selected changes with publication and effective dates, the GMP processes potentially affected, and a link to verify each at the issuing authority.
Open the calendarChange impact analyser
Select the GMP areas a change plausibly touches and get a consolidated review checklist: what to review, which evidence to re-examine and the questions to answer.
Analyse a changeSource library
The authorities themselves — European Commission and EudraLex, EMA, IGJ, PIC/S, ICH, MHRA and FDA — with official text kept separate from our explanation.
Browse sourcesRegulatory news
Guidance changes and inspection trends with the practical consequence attached, rather than a summary of the text.
Read the newsWork out what a change means for your site
Start from the calendar to see what changed, then use the analyser to scope the review across the GMP areas it touches.