FACTS ON VARIATION FILING IN EUROPEAN UNION

29th July, 2014 - Posted by Rahul Agarwal - No Comments

FACTS ON VARIATION FILING IN EUROPEAN UNION The regulatory authorities generally demand continuous up gradation of quality, indication, safety of the drug products. To achieve this they have framed variation guidelines which cover minor to major variations. The guidelines are also useful for registering minor administrative changes. How variations are classified in EU and who […] Share this:LinkedInFacebook Read More