Author(s): B. Jayalakshmi, R. Seetharaman, R. Kamaraj

Email(s): jayaranijini3017@gmail.com

DOI: 10.5958/0974-360X.2019.00234.8   

Address: B. Jayalakshmi, R. Seetharaman, R. Kamaraj*
Department of Pharmaceutical Regulatory Affairs, SRM Institute of Science and Technology,
SRM College of Pharmacy, Kattankulathur-603203 Dist–Kancheepuram, India
*Corresponding Author

Published In:   Volume - 12,      Issue - 3,     Year - 2019


ABSTRACT:
The comparative study of generic drug registration in BRICS, was to find out the differences among the guidelines. “BRICS” mainly refers to Brazil, Russia, India, china and South Africa. The regulatory requirements of each country is different from each other, “BRICS” has the fastest growing and largest emerging markets which shows the positive growth in the pharmaceutical companies. The medical regulatory system in the BRICS countries is increasing in the medical profession to safeguard and promote the medicine. The BRICS countries together is consider as important emerging economics, which has 40% of world population. To develop the universal health coverage, The BRICS countries of national institution agreed to join hands with (WHO), world health organization.


Cite this article:
B. Jayalakshmi, R. Seetharaman, R. Kamaraj. Registration and Regulatory Requirements of Generic Drugs Marketing Authorization in “BRICS” Countries. Research J. Pharm. and Tech. 2019; 12(3): 1403-1408. doi: 10.5958/0974-360X.2019.00234.8

Cite(Electronic):
B. Jayalakshmi, R. Seetharaman, R. Kamaraj. Registration and Regulatory Requirements of Generic Drugs Marketing Authorization in “BRICS” Countries. Research J. Pharm. and Tech. 2019; 12(3): 1403-1408. doi: 10.5958/0974-360X.2019.00234.8   Available on: https://rjptonline.org/AbstractView.aspx?PID=2019-12-3-73


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