Comparative study of medicinal products registration in USA and Europe

https://doi.org/10.54037/WJPS.2022.100303

Authors

  • K. Vamsi Priya Department of Regulatory Affairs, Krishna Teja Pharmacy College, Chadalawada Nagar, Renigunta Road, Tirupathi, Andhra Pradesh-517506
  • K. Umasankar Department of Regulatory Affairs, Krishna Teja Pharmacy College, Chadalawada Nagar, Renigunta Road, Tirupathi, Andhra Pradesh-517506
  • J. Praveen Kumar Department of Regulatory Affairs, Krishna Teja Pharmacy College, Chadalawada Nagar, Renigunta Road, Tirupathi, Andhra Pradesh-517506
  • M. Kishore Babu Department of Regulatory Affairs, Krishna Teja Pharmacy College, Chadalawada Nagar, Renigunta Road, Tirupathi, Andhra Pradesh-517506

Keywords:

USFDA, Regulatory Affairs, Pharmaceuticals

Abstract

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.

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Published

2022-03-01

How to Cite

K. Vamsi Priya, K. Umasankar, J. Praveen Kumar, & M. Kishore Babu. (2022). Comparative study of medicinal products registration in USA and Europe: https://doi.org/10.54037/WJPS.2022.100303. World Journal of Pharmaceutical Sciences, 10(03), 263–266. Retrieved from https://wjpsonline.com/index.php/wjps/article/view/comparative-study-medicinal-products-registration-usa-europe

Issue

Section

Research Article