What is Mean by Drug Master File I/II : Introduction/ Description: Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority...
This article contains the list of Global Drug Regulatory Authorities. What is mean by Drug Regulatory Authorities and what are there Roles: Drug Regulatory Authorities are a government authorities have responsibility for granting licenses,...
This article contains the Differentiation between Good manufacturing practices (GMP) and Current Good manufacturing Practices (cGMP). Differentiation of GMP Vs cGMP Introduction : GMP and cGMP are crucial regulations in the pharmaceutical industry to...
