Which sites the EU has found significantly non-compliant.
When an EU supervisory authority inspects a manufacturer and finds serious GMP failures, it publishes a statement of non-compliance in EudraGMDP — the European counterpart to an FDA warning letter. SPEQ tracks each recent report with its site, country, reference, and a link to the full statement.
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EU GMP non-compliance reports from EudraGMDP — the European counterpart to a warning letter. Track EMA and SPEQ sends you one weekly email with what it published — nothing on a quiet week — so the bodies you answer to sit in one place instead of across a dozen tabs.
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How to use this library
This is the EU’s equivalent of a warning letter: a statement of GMP non-compliance entered on EudraGMDP after an inspection. Narrow by country, then open a report for its reference, date and a link to the EudraGMDP entry.
Reports are EudraGMDP records reproduced as published; SPEQ adds no interpretation. A statement of non-compliance concerns the inspected site at the time of inspection and is not a statement about a company’s other sites or its current status.
COMPLETE INDEX — ALL 13 NON-COMPLIANCE REPORT
Every count on this page is derived from the eu_gmp_noncompliance table at render — none is a literal. Follow each reference for the authoritative EudraGMDP entry.
Source: EudraGMDP GMP Non-Compliance Report search (eudragmdp.ema.europa.eu), scraped andrefreshed daily. Reports are EU regulator records reproduced as published — SPEQ adds no interpretation. The archive builds forward from the first scan.
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