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How to conduct product quality review in pharmaceutical

GMPSOP

NOVEMBER 19, 2023

You should perform product quality review annually to determine if any adjustments to product specifications, manufacturing process or raw material supply are required to improve the product further. The content of this article does not supersede or replace any local or international regulatory requirements. Subscribe f.

Documentation 52
Documentation Packaging Method Validation Process Improvement 52
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Corrective and Preventive Action (CAPA) Procedure for GMP

GMPSOP

MARCH 17, 2023

Table of Contents If you are looking for literary help to write an actionable procedure on corrective and preventive action for your workplace or school, this article will be a good place to start. Further to corrective action, the defective packaging (carton) lot was destroyed which was initially quarantined. Consider this scenario.

Documentation 52
Documentation Packaging Process Improvement Pharmaceutical Manufacturing 52
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