Open AccessComparative study of medicinal products registration in USA and Europe
Author(s) -
K. Vamsi Priya,
K. Umasankar,
J. Praveen Kumar,
M. Kishore Babu
Publication year - 2022
Publication title -
world journal of pharmaceutical sciences
Language(s) - English
Resource type - Journals
eISSN - 2321-3310
pISSN - 2321-3086
DOI - 10.54037/wjps.2022.100303
Subject(s) - cosmetics , regulatory affairs , business , quality (philosophy) , health care , medicine , risk analysis (engineering) , political science , public administration , law , pathology , philosophy , epistemology
A pharmaceutical drug regulatory Affairs is mainly involved in registration process parameters of different pharmaceutical products and new drug application. Regulatory affairs professionals play vital roles in a pharmaceutical field as; it is related to healthcare products. The present article mainly focuses to provide similarities and differences in the registration of medicinal products in USA and European countries.This also provide details to protect public health in terms of safety, quality, and efficacy of products like medical devices, pharmaceuticals, veterinary medicines, pesticides, cosmetics & complementary medicines, agrochemicals, etc.