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[ EU · GMP NON-COMPLIANCE REPORTS ]

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.

14
Reports tracked
24 Jun 2026
Most recent
8
Countries
India · 4Netherlands · 3China · 2Italy · 1Spain · 1Sri Lanka · 1
24 Jun 2026Italy
Avlab S.r.l.
Ref: IT/NCR/01/H/2026
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17 Jun 2026Spain
Laboratorios Eurisko S.L.
Ref: PE010-5017
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24 Apr 2026China
Sichuan New Hawk Biotechnology Co. Ltd.
Ref: INS-484650-105391479-21678300
View details →
21 Apr 2026Netherlands
Produlab Pharma B.V.
Ref: V2059716 2026-3158557
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21 Apr 2026Sri Lanka
Navesta Pharmaceuticals (Pvt) Ltd.
Ref: MT/003NCR/2026
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21 Apr 2026Netherlands
Veyx-Pharma B.V.
Ref: V2059716 2026-3158557
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21 Apr 2026Netherlands
Produlab Pharma Production B.V.
Ref: V2059716 2026-3158557
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31 Mar 2026India
Zenzi Pharmaceutical Industries Private Limited
Ref: MT/002NCR/2026
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18 Mar 2026India
Cadchem Laboratories Limited
Ref: NNGYK/34812-5/2026
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13 Mar 2026India
Swiss Parenterals Limited
Ref: 530-10/26-06/03; 381-13-08/366-26-06
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13 Mar 2026India
Swiss Parenterals Limited
Ref: 530-10/26-06/04; 381-13-08/310-26-06
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12 Feb 2026China
Bio-Thera Solutions Ltd.
Ref: 2026_NCR_MEDBIO_003
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29 Oct 2025Portugal
Technophage Investigacao E Desenvolvimento Em Biotecnologia S.A.
Ref: F068/S1/ME/001/2024/NCR
View details →
5 Sept 2025United States
Intervet Inc.
Ref: NL/V 25/2056902
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Source: EudraGMDP GMP Non-Compliance Report search (eudragmdp.ema.europa.eu), scraped and refreshed daily. Reports are EU regulator records reproduced as published — SPEQ adds no interpretation. The archive builds forward from the first scan.