Open AccessGood Manufacturing Practice (GMP): History, structure and its significance
Author(s) -
Abhimanyu Rampal,
S. P. Yamini Kanti
Publication year - 2020
Publication title -
international journal of drug regulatory affairs
Language(s) - English
Resource type - Journals
eISSN - 2321-7162
pISSN - 2321-6794
DOI - 10.22270/ijdra.v8i4.439
Subject(s) - good manufacturing practice , harm , product (mathematics) , cosmetics , order (exchange) , business , medical practice , risk analysis (engineering) , set (abstract data type) , population , medicine , computer science , marketing , environmental health , intensive care medicine , law , mathematics , programming language , supply chain , geometry , finance , pathology , political science
Good Manufacturing Practice (GMP) is set of guidelines enforced by USFDA under 21 CFR. Every Manufacturer of Food, Cosmetics, Pharmaceuticals products, Medical Devices & Dietary products should follow these guidelines in order to be sure that their product is safe and effective to be put in the market and for use by general population. The parameters of GMP for different Categories may vary but there is only one aim & that is to prevent any kind of harm that can occur to the final user of the product.