RULES AND REGULATIONS CONCERNED WITH AYURVEDIC PHARMACY IN INDIA
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Abstract
one of the oldest systems of medicine, has gained renewed attention in recent years due to its holistic approach and minimal side effects. With this resurgence, Ayurvedic pharmaceuticals have emerged as a prominent industry. However, to ensure safety, efficacy, and quality, the Government of India has laid down comprehensive rules and regulations governing the manufacturing, marketing, and sale of Ayurvedic medicines. This article explores the major legal frameworks, regulatory bodies, and compliance procedures that govern Ayurvedic pharmacy in India.
References
2. Schedule T: Good Manufacturing Practices for Ayurvedic, Siddha, and Unani Drugs. Included in the Drugs and Cosmetics Rules, 1945.
3. Ayurvedic Pharmacopoeia of India (API). Published by Pharmacopeial Commission for Indian Medicine & Homoeopathy (PCIM&H).
4. Ayurvedic Formulary of India (AFI). Published by Ministry of AYUSH, Government of India.
5. Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954. Available at: https://legislative.gov.in
6. Guidelines for Licensing of ASU Drugs. Ministry of AYUSH, Government of India. Available at: https://ayush.gov.in
7. Ministry of AYUSH Notification on Proprietary Ayurvedic Medicines. Government of India.
8. Pharmacopeial Commission for Indian Medicine & Homoeopathy (PCIM&H). Website: https://pcimh.gov.in
9. National Accreditation Board for Testing and Calibration Laboratories (NABL). Website: https://nabl-india.org
10. Guidelines for Good Clinical Practices and Research in AYUSH. Issued by CCRAS and Ministry of AYUSH.
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Dr. Ranjit Kumar
MD Scholar, Department of Rasashastra & Bhaishajya Kalpana, Government Ayurvedic College and Hospital Patna, Bihar, India
Dr. Prabhat Kumar Dwivedi
Professor, Department of Rasashastra & Bhaishajya Kalpana, Government Ayurvedic College and Hospital Patna, Bihar, India