Author(s): Harit Kasana, Harish Chander, Ashwani Mathur

Email(s): ashwani.mathur@mail.jiit.ac.in

DOI: 10.52711/0974-360X.2024.00378

Address: Harit Kasana1,2, Harish Chander1, Ashwani Mathur2
1National Institute of Biologicals (Ministry of Health and Family Welfare, Government of India) A-32, Sector - 62, Noida - 201309, India.
2Department of Biotechnology, Jaypee Institute of Information Technology, Noida, A-10, Sector - 62, Noida, 201309, Uttar Pradesh, India.
*Corresponding Author

Published In:   Volume - 17,      Issue - 5,     Year - 2024


Cite this article:
Harit Kasana, Harish Chander, Ashwani Mathur. A Systematic Review of Regulatory requirements of Biosimilar Products: WHO, India, European Union and USFDA. Research Journal of Pharmacy and Technology. 2024; 17(5):2413-0. doi: 10.52711/0974-360X.2024.00378




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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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