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How to conduct product quality review in pharmaceutical

GMPSOP

NOVEMBER 19, 2023

Trending will help identify product and process improvements. Component quality A review of all starting materials and primary packaging in contact with the product should be completed. You must have a summary of all complaints or adverse events during the review period. 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

Corrective and preventive actions are identified and implemented as the outcome of investigations such as deviations, product complaints, internal audit observations, risk assessments, stability failure, or other process or system-related non-conformances. The entire unused packaging lot which was quarantined was returned to the supplier.

Documentation 52
Documentation Packaging Process Improvement Pharmaceutical Manufacturing 52
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