An Overview of Drug Regulatory System in India
Prerana Husukale
, Dr.I.D.Gonjari
Regulatory affair, Safety, Efficacy, Quality, CDSCO, DTAB, DCC.
Pharmaceutical drug regulatory affairs encompass a variety of pharmaceutical product registration parameters. As a new profession, it arose from the desire of people all over the world to protect public health by providing high-quality medicine, including safety and efficacy, in areas such as veterinary medicine, medical devices, insecticides, pesticides, agrochemicals, cosmetics, and complementary medicine. It also served as a link between the pharmaceutical industry and regulatory bodies. It's also in charge of making sure the product information is up to date and accurate. Its primary responsibility is to function as a liaison with regulatory bodies, offering experience and regulatory intelligence in translating regulatory requirements into a practical, workable strategy, and advising the company on regulatory elements and climate that may affect their intended actions.
"An Overview of Drug Regulatory System in India", IJSDR - International Journal of Scientific Development and Research (www.IJSDR.org), ISSN:2455-2631, Vol.7, Issue 6, page no.71 - 74, June-2022, Available :https://ijsdr.org/papers/IJSDR2206010.pdf
Volume 7
Issue 6,
June-2022
Pages : 71 - 74
Paper Reg. ID: IJSDR_200528
Published Paper Id: IJSDR2206010
Downloads: 000347032
Research Area: Pharmacy
Country: Stara, Maharashtra, India
ISSN: 2455-2631 | IMPACT FACTOR: 9.15 Calculated By Google Scholar | ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 9.15 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator
Publisher: IJSDR(IJ Publication) Janvi Wave