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Call Us Anytime 0731-2492054
Welcome to Mehta Ayurvedic Sansthaan — an Ayush-licensed manufacturing institution built on compliance and scientific alignment.
Licensed under Ministry of Ayush since 1985, MAS operates with ISO 9001:2015 and GMP-certified systems. Every formulation is manufactured within documented regulatory frameworks with complete batch traceability.
Through structured collaborations with leading research institutions, MAS supports analytical standardization, mechanism-of-action studies, and evidence-building initiatives for clinical and institutional integration.
Designed for hospitals, healthcare institutions, and compliant private-label partners, MAS provides documented manufacturing, quality dossiers, and long-term supply planning under NDA and formal agreements.
Our product portfolio extends beyond spearhead formulations to encompass a broad range of clinically relevant, evidence-based Ayurvedic cannabis
solutions, catering to a wide spectrum of patient conditions and preferences.
-Fast-acting oils for acute pain & anxiety
-Tablets for sustained relief in chronic
conditions
-Standardized cannabinoid ratios for
consistent effects
Our product portfolio extends beyond spearhead formulations
No.
Mehta Ayurvedic Sansthaan operates exclusively as a B2B manufacturing partner. We do not process retail orders or individual purchase requests.
MAS collaborates with hospitals, institutional buyers, research bodies, healthcare practitioners, and private-label brands operating within regulated frameworks.
Yes.
MAS holds Ministry of Ayush licensing for processing Vijaya (Cannabis) formulations and operates under ISO 9001:2015 and GMP-certified systems.
Every manufacturing batch is supported by:
• Certificate of Analysis (COA)
• Potency testing
• Microbial analysis
• Heavy metals screening
• Pesticide residue testing
Full batch traceability is maintained for audit readiness.
Yes.
Custom formulation development is available under NDA, subject to regulatory alignment and technical feasibility assessment.
Engagement follows a structured process:
Initial inquiry
Requirement mapping
NDA execution
Technical review
Commercial discussion
Four decades of regulated manufacturing experience, early licensure in medicinal cannabis processing, documented quality systems, and alignment with scientific validation frameworks.