DRUG REGULATORY AFFAIRS IN QUALITY MANAGEMENT

Registration ID: IJNRD_187681

Published ID: IJNRD2302234

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Indra Kumar Dubey, Shivraj Singh Bhadauriya

Regulatory authorities, role of regulatory affairs department, responsibility of regulatory affairs professionals, regulatory requirements for drug approval.

Pharmaceutical drug regulatory affairs govern registration parameters of pharmaceutical products. It has a broad spectrum covering all aspects of documentation and marketing in legalized form. The pharmaceutical industry is highly regulated industries in our country. Regulatory affairs professionals are need of present market scenario to cater to link pharmaceutical industries and worldwide regulatory agencies. Regulatory affairs, is a profession within synchronized various industries, such as pharmaceuticals, medical devices and biotechnological industries. Regulatory affairs also have a very specific meaning within the pharmaceutical industries. Quality management is an approach to maximize competitiveness of an organization through continuous improvement of its product, services, people, process and environment. The best environment to produce quality products is the safe and healthy environment.

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Indra Kumar Dubey & Shivraj Singh Bhadauriya (February-2023). DRUG REGULATORY AFFAIRS IN QUALITY MANAGEMENT. INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT, 8(2), c265-c282. https://ijnrd.org/papers/IJNRD2302234.pdf

Volume 8 Issue 2, February-2023

Pages : c265-c282

Paper Reg. ID: IJNRD_187681

Published Paper Id: IJNRD2302234

Downloads: 000122253

Research Area: Pharmacy

Author Type: Indian Author

Country: Bhadohi, Uttar Pradesh, India

Published Paper PDF: https://ijnrd.org/papers/IJNRD2302234.pdf

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Journal Name: INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT(IJNRD)

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