The field of Ayurveda, one of the oldest systems of traditional medicine, has witnessed significant global growth in recent decades. With increasing commercialization and international acceptance, there is a rising need to align Ayurvedic practices with modern regulatory frameworks to ensure safety, efficacy, and quality of products. Regulatory affairs in Ayurveda involve compliance with national and international laws, including product registration, labeling, clinical validation, and good manufacturing practices (GMP). In India, the Ministry of AYUSH plays a central role in regulating Ayurvedic medicines, while internationally, products often face scrutiny under the laws of countries where traditional medicine is not formally integrated. This study aims to provide an overview of the current regulatory landscape governing Ayurveda and presents findings from a survey conducted among Ayurvedic practitioners, manufacturers, and regulatory professionals. The survey explores awareness levels, challenges faced in regulatory compliance, and perspectives on harmonization of traditional and modern health regulations. Results reveal key gaps in knowledge, limited access to regulatory resources, and a strong demand for updated training programs. The findings underscore the need for enhanced policy frameworks and stakeholder education to foster safe, effective, and compliant growth of the Ayurvedic sector.