E-Aushadhi Registration

E-Aushadhi is an online portal mandated by the government for the licensing, registration, and regulatory compliance of Ayurveda, Siddha, and Unani (ASU) drugs. It ensures transparency and streamlines the application process.

Yes, we provide end-to-end documentation preparation, technical guidance, and compliance support for acquiring new Ayurvedic Manufacturing Licenses through the E-Aushadhi portal.

A Loan License allows you to manufacture your products at another company's approved facility. We handle the documentation, compliance verification, and technical coordination between your brand and the manufacturing unit.

Timelines vary depending on the application type (new license, renewal, or product permission) and document readiness. However, our expert guidance ensures accurate, first-time submissions to prevent rejections and expedite the approval process.

Absolutely. We review your existing products and documents, perform technical corrections, and provide E-Aushadhi data correction and verification support to ensure smooth regulatory transitions.

Yes, we collaborate closely with NABL-approved laboratories to coordinate stability studies, ensuring your shelf-life documentation meets all domestic and international export requirements.

We offer comprehensive export documentation support including COA (Certificate of Analysis) coordination, Free Sale Certificates assistance, product specifications, and stability & technical dossiers.

Yes, regulatory authorities require all legacy product data, past approvals, and old licenses to be digitized and continuously updated on the E-Aushadhi portal to maintain legal compliance.