Schedule T includes detailed guidelines and mandatory requirements covering the following core components: Components of GMP (Schedule T) Infrastructural Requirements GMP mandates that the manufacturing facility should be properly designed to facilitate smooth workflow and prevent contamination. Building Design: Must have a well-planned layout to separate different manufacturing sections. Ventilation & Lighting: Adequate ventilation, air … Read more
What is Schedule T? Schedule T is a section of the Drugs and Cosmetics Act, 1940, outlining Good Manufacturing Practices (GMP) for Ayurveda, Siddha, and Unani (ASU) medicines. It sets standards for manufacturing, storage, and distribution to ensure safety, consistency, and quality in herbal medicines. Objectives of Schedule T Ensure Quality & Safety – Prevents … Read more
Institutions Involved in Research & Development of Medicinal & Aromatic Plants in India explain roles research support and contributions to herbal drug development. Institutions Involved in Research & Development of Medicinal & Aromatic Plants in India Several institutions in India focus on research, conservation, and development of medicinal and aromatic plants. Some of the key … Read more
Plant-Based Industries Involved in Medicinal & Aromatic Plants in India explains sectors scope cultivation processing and market role. Plant-Based Industries Involved in Medicinal & Aromatic Plants in India India is one of the largest producers and exporters of medicinal and aromatic plants. Several industries are directly or indirectly involved in the processing and commercialization of … Read more
Herbal Drugs Industry: Present Scope and Future Prospects Herbal Drugs Industry: Present Scope and Future Prospects explains current scope growth trends and future potential of herbal medicines. Introduction The herbal drugs industry, also known as the phytomedicine industry, is rapidly expanding due to increasing demand for natural and organic products. With a rich history in … Read more
General Introduction to Herbal Industry explains scope growth regulatory framework and role of herbal medicines in healthcare systems. General Introduction to Herbal Industry The herbal industry refers to the sector that deals with the cultivation, processing, manufacturing, and commercialization of plant-based products used for medicinal, therapeutic, cosmetic, and nutritional purposes. This industry is an integral … Read more
Schedule Z of the Drugs & Cosmetics Act for ASU Drugs explains regulatory requirements quality standards and documentation for ASU medicines. Schedule Z of the Drugs & Cosmetics Act for ASU Drugs Schedule Z outlines regulatory requirements for conducting clinical trials on Ayurvedic, Siddha, and Unani (ASU) medicines to ensure their safety, efficacy, and therapeutic … Read more
Regulation of ASU Drug Manufacture in India explains legal framework standards licensing and quality control of traditional medicines. Regulation of ASU Drug Manufacture in India The manufacturing of Ayurveda, Siddha, and Unani (ASU) drugs in India is governed by: Drugs and Cosmetics Act, 1940 Drugs and Cosmetics Rules, 1945 (with amendments specific to ASU drugs) … Read more
ASU Drugs Consultative Committee (ASU-DCC) ASU Drugs Consultative Committee (ASU-DCC) explains role functions and regulatory importance in traditional medicine drug governance. Establishment and Legal Basis: Constituted under Section 33D of the Drugs and Cosmetics Act, 1940. Functions as a consultative body for central and state governments. Composition The ASU DCC consists of representatives from: State … Read more
Establishment and Legal Basis: Constituted under Section 33D of the Drugs and Cosmetics Act, 1940. Functions as a consultative body for central and state governments. Composition The ASU DCC consists of representatives from: State governments and union territories Central regulatory authorities Domain experts in ASU drug regulation Mandate and Functions Harmonization of Enforcement – Ensures … Read more
