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Drug Regulation in India: India is one of the largest manufacturers of drugs and exports pharmaceutical products to over 200 countries/economies.As India has a federal form of government, so the medical regulatory structure is divided between national and state authorities. Medicines in India are regulated by CDSCO – Central Drugs Standard Control Organization under Ministry of Health and Family Welfare. Headed by Directorate General of Health Services CDSCO regulates the Pharmaceutical Products through DCGI – Drugs Controller General of India at Chair.
Functions of CDSCO:
Pharmaceutical Regulation
The term ‘pharmaceuticals regulation’ means the regulation of any aspect of the production, distribution, prescription or consumption of a pharmaceutical product or the raw materials that are used in its production.
Major Issues in Indian Regulatory System:
Most worrisome issue
Major Roadblock The Pharmaceutical industry is politically very powerful and it has used all its influence in the past to block reforms initiated by the Government.
Effect of poor drug regulations
Recent steps taken by the Government to Strengthen and Upgrade our drug regulatory system
What else can be done? We need to make centralised licensing because States lack the necessary resources to coordinate their activities among themselves, and this loophole is exploited by the manufacturers.
By: ABHISHEK KUMAR GARG ProfileResourcesReport error
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