Revised GMP principles by EU on Qualification and Validation

New Delhi February 17, 2014:- Good manufacturing practices guidelines are of significant importance to provide guidance for interpretation of principles and guidelines of qualification and validation applicable to the facilities, equipments, utilities and processes used for the manufacture of medicinal products. According to new draft from European Commission for GMP guidelines, the manufacturers of the drug products should assure the critical parameters of their processes through qualification and validation of the product and process.