Feature Article
Advantages of a good deviation/Incidence handling System
By : Francis Fernandes and Dr. Subhash Pande
The purpose of various Quality Assurance, GMP and Documentation Systems in pharmaceutical industry is to ensure quality and safety of the products manufactured .Such practices and systems are not stand alone systems. They are all linked to each other. For example: A Deviation done during the manufacturing leads to an Investigation to identify the cause for the deviation .Once the cause is identified, corrective and preventive actions are taken to avoid the re occurrence [ CAPA] that may require to undergo a Change management system and all these are finally reported in the Annual Product reviews, prepared on the yearly basis…
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