<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>162</id><JournalTitle>A COMPREHENSIVE STUDY OF REGULATORY MEASURES TO EFFECTIVELY PREVENT THE SPURIOUS ADULTERATED AND LOW QUALITY DRUGS</JournalTitle><Abstract>The existing bifurcated regulatory framework, comprising the State Drug Control Departments (SDCD) and the Central
Drugs Standard Control Organization (CDSCO), is fraught with inefficiencies and inconsistencies, undermining the
effectiveness of drug regulation in India. The proposal to merge these entities into a single, unified Drug Regulatory
System presents a comprehensive solution to these systemic shortcomings. This consolidation will ensure the uniform
implementation of The Drugs & Cosmetics Act, 1940, and its associated rules, effectively addressing the prevalence of Not
of Standard Quality (NSQ), spurious, and adulterated drugs. By centralizing regulatory oversight, the responsibility for
ensuring drug quality in the domestic market and for exports will be streamlined and enhanced. Additionally, this
integrated approach is poised to catalyze significant growth in the Indian pharmaceutical and allied industries, positioning
them as global leaders in the near future</Abstract><Email>dravinashreddy88@gmail.com</Email><articletype>Research</articletype><volume>14</volume><issue>1</issue><year>2024</year><keyword>Drug Regulation, Unified System, Drugs & Cosmetics Act, 1940, NSQ Drugs, Pharmaceutical Growth</keyword><AUTHORS>Vennam Venkatadri1, Avinash Kumar G, Dinakar A, Manasa E</AUTHORS><afflication>1Department of Pharmaceutics, Sun Institute of Pharmaceutical Education and Research, Kakupalli, Nellore-524346, Andhra Pradesh, India</afflication></Article></Articles>