Remove Labelling Remove Pharmaceutical Manufacturing Remove Process Improvement
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IPA questions FAERS data interpretation in the Ohio State University study

Express Pharma

It attributed Indias cost advantage to high-production capacity plants, process improvements, economies of scale, and backward integration in manufacturing. IPA also addressed concerns regarding transparency in drug manufacturing locations.

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Corrective and Preventive Action (CAPA) Procedure for GMP

GMPSOP

– Status control: implementing status labels to clearly identify workflow status such as issues, returns, rejects and reworks of components to prevent mix ups. For instance, you can undertake a list of process improvement works targeting the elimination of causes that have resulted in the defect.