Vol. 3, Issue 1, Part A (2026)

The standardization of Ayurvedic medicines plays a crucial role in ensuring their efficacy, safety, and quality in modern healthcare systems. As traditional practices have evolved, the need to adapt Ayurvedic formulations to scientific standards has become essential. Standardization involves rigorous methods that focus on the accurate assessment of raw materials, formulation processes, and final products. Techniques such as chromatographic methods, high-performance liquid chromatography (HPLC), mass spectrometry, and molecular biology tools are being increasingly applied to enhance the precision of quality control measures. Additionally, the development of pharmacopoeial standards, clinical trials, and regulatory frameworks is necessary to ensure that Ayurvedic medicines meet the global pharmaceutical standards. The challenges faced in standardizing Ayurvedic medicines are multifaceted, including the diversity of raw materials, variations in geographical conditions, and the lack of universally accepted protocols. However, the integration of modern scientific approaches with traditional Ayurvedic knowledge provides a promising avenue for improving the reliability of these medicines. The objective of this review is to explore the various approaches and techniques employed in the standardization of Ayurvedic medicines, and to propose a pathway for ensuring their authenticity and reproducibility. This paper also highlights the ongoing developments and future directions in the standardization process, contributing to the harmonization of Ayurveda with global health practices.