NOT KNOWN DETAILS ABOUT PHARMA REGULATORY AUDITS

Not known Details About pharma regulatory audits

In line with ISO 9000:2015, the pharmaceutical company is accountable for taking motion and controlling the nonconformities. In addition, it calls for the company to eliminate the cause of the nonconformity by:Since each and every company would like to focus on manufacturing, And through manufacturing, cGMP violations will not be unusual. These vio

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good documentation practices - An Overview

Any superseded learn documents and Sequential logbook of past months/year, paperwork of prior 12 months and aged documents shall be retained at File Area According to Annexure 10.Any questionable or deteriorated circumstances that happen to be pointed out shall bring to the attention of your Section Head.Hold all the completed data files of your do

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