Inspection Record

Avenza Pharmaceuticals Private Limited — EU GMP NCR (EudraGMDP) Findings

EMA (Europe)Inspected 2023-08-25Published 2024-08-02 1 findingComputer system validation

View the regulator's official source The source document is always the basis for judgement.

Findings

1Computer system validation

This Statement of GMP Non-compliance relates to proposed activities at the Avenza Pharmaceuticals Pvt. Limited site identified above. The company was not compliant with EU-GMP standards. At the time of the inspection the process for manufacture of Paracetamol Tablets had not been appropriately validated, the cleaning process had not been appropriately validated and the inventory management system had not been fully validated. Inspection Outcome: Seven major deficiencies were identified during the inspection. These related to the following areas: • Management of computerized systems. • Cleaning Validation • Process Validation • Physical/Chemistry Laboratory • Investigation of OOS Results • Management of the stability program • Vendor Qualification and Management Action taken/proposed by the NCA: Others Importers variation withdrawn.

About this record

Extracted automatically from the document EMA (Europe) published on 2024-08-02. The source is available at the link above.

This is a record of that moment. Inspection findings are usually followed by the company's response and corrective action, but this page does not know how that turned out. Do not read it as the current state; check the regulator's official announcements for the latest status.

Translation and classification are automated and may differ in nuance from the source.

Avenza Pharmaceuticals Private Limited company profile — full historyAll EMA (Europe) findings EMA (Europe) documents, 2024 Go to Findings search
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