The programme was aimed at strengthening the regulatory framework, quality assurance, and standardisation processes for Ayurveda, Siddha, Unani, and Homoeopathy drugs.
Photo: X/@PIB_India
The Pharmacopoeia Commission for Indian Medicine & Homoeopathy (PCIM&H), Ministry of Ayush, conducted a five-day capacity building training programme from September 8 to 12 at its headquarters in Ghaziabad.
The programme was aimed at strengthening the regulatory framework, quality assurance, and standardisation processes for Ayurveda, Siddha, Unani, and Homoeopathy drugs.
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The training brought together 27 participants from across India, representing regulatory bodies, research councils, pharmaceutical industries, and academic institutions.
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The comprehensive sessions were designed to equip Drug Enforcement Officers, Quality Control Personnel, and drug manufacturers with advanced knowledge and hands-on experience in pharmacopoeial standards and Good Manufacturing Practices.
The programme was inaugurated by Prof (Vaidya) Rakesh Sharma, Former President, Board of Ethics & Registration, NCISM. Dr Tarkeshwar Jain, Former President, Homoeopathy Education Board, NCH, graced the occasion as Guest of Honour. The inaugural session was led by Dr Raman Mohan Singh, Director, PCIM&H.
Participants highly appreciated the programme’s unique blend of expert-led lectures, practical laboratory sessions, and field visits. The training significantly contributed to enhancing their understanding of Pharmacopoeial Standards, GMP, and Regulatory Compliance, thereby reinforcing the national commitment to ensuring the safety, efficacy, and quality of ASU&H drugs.
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