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

The formulation and development of Ayurvedic formulations, rooted in ancient traditions, faces several challenges in the modern pharmaceutical landscape. Despite the growing interest in holistic and alternative healthcare, Ayurvedic formulations often encounter barriers such as standardization, quality control, regulatory compliance, and scientific validation. These challenges stem from the complex nature of Ayurvedic formulations, which often involve a variety of plant-based ingredients, mineral compounds, and animal products. The absence of uniform guidelines and methodologies for quality assurance contributes to the difficulty in ensuring consistency and safety in the production of Ayurvedic drugs. Furthermore, the lack of robust clinical trials and scientific evidence supporting their efficacy hinders the acceptance of Ayurvedic medicine within the global healthcare framework.
This paper explores the key challenges faced in the formulation and development of Ayurvedic formulations, emphasizing issues related to quality control, formulation standardization, and scientific validation. Additionally, it highlights potential solutions, such as the integration of modern technological advancements in pharmacognosy, analytical methods for quality assurance, and the need for stringent regulatory policies. The objective of this paper is to propose a strategic framework for overcoming these challenges, with the hypothesis that standardization and scientific validation are essential for the future growth and acceptance of Ayurvedic formulations in mainstream healthcare.
Through a comprehensive review of the literature, this paper aims to provide insights into how the Ayurvedic industry can innovate and align with modern pharmaceutical standards while maintaining its traditional healing principles. Ultimately, it strives to contribute to the advancement of Ayurvedic medicine by addressing existing barriers and identifying practical solutions for its integration into global health systems.