Availability of Standard Quality Drugs Ensured in India: Stringent Drug Regulations and Up Graded Regulatory Mechanism
Author:
Affiliation:
1. Chitkara College of Pharmacy, Chitkara University, Punjab, India.
2. School of Pharmaceutical Sciences, Lovely Professional University, Jalandhar-Delhi G.T Road, Phagwara, Punjab, India.
3. Independent Researcher, Mohali, Punjab, India.
Abstract
Publisher
A and V Publications
Reference27 articles.
1. World Health organization’s Substandard and falsified medical products report available on https://www.who.int/news-room /questions-and-answers/item /substandard-and-falsified-medical-products-scope-scale-and-harm. Accessed on 10th Jan. 2023.
2. Sunitha D, Hemalatha K, Sudhakar M. Banned Drugs: A Review. Asian Journal of Pharmaceutical Research. 2016; 6(4): 205-16.
3. Anuradha VP, Joseph B, Jayakrishnan SS, Ajith B. Black Triangle Drugs. Asian Journal of Pharmaceutical Research. 2019; 9(3): 203-5.
4. Poovarasan D, Manikandan K, Kamaraj R. Regulatory Requirement and Registration Process of Generic Drugs in Japan. Research Journal of Pharmacy and Technology. 2020; 13(3): 1523-6.
5. Indian Council for Research on International Economic Relations’ web site available on https://icrier.org/pdf/PolicyBrief_%202_health.pdf. Accessed on 12th Jan. 2023.
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