Regulatory Framework for Ayush Medicines
India's regulatory framework for Ayurveda, Siddha, and Unani (ASU) medicines is guided by the Drugs Rules, 1945, which ensures safety, quality, and efficacy. Manufacturers must comply with licensing requirements and Good Manufacturing Practices (GMP). Drug testing laboratories and pharmacovigilance centres play critical roles in maintaining standards and monitoring safety. Quality control is overseen by the Ministry of Ayush through the PCIM&H. Misleading advertisements are regulated under the Drugs and Magic Remedies Act, 1954. The framework supports research initiatives and ethical guidelines, reinforcing the credibility of traditional medicine systems while encouraging scientific validation.
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