CLEANING VALIDATION WORKSHOP 2016

With the increase in scrutiny by US FDA, the Indian Pharmaceutical Industry is striving to comply with the cGMP guidelines. In order to ensure failure free compliance, it is a must for the pharmaceutical manufacturers to validate its cleaning processes to avoid cross contamination and ensure safety and efficacy of the drug products. Looking at the criticality of understanding the regulatory authority’s expectations and to determine efficient execution of the cleaning process, CPhI is organising a Cleaning Validation Workshop which is scheduled from June 23 – 24, 2016 in Mumbai.

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