Manufacture traditional medicines legally with Ayush Licence.
An Ayush Licence issued under the Drugs and Cosmetics Act, 1940 is mandatory for manufacturing, distributing, and selling Ayurvedic, Unani, Siddha, and Homeopathic products in India. We manage the complete State Licensing Authority application, GMP compliance, and inspection coordination.
Pricing
Pricing tailored to your specific requirements
Ayush Licence Obtained in 15 Days*
*Timeline is indicative and may vary based on document verification and government processing.
What is an Ayush Licence?
An Ayush Licence is issued by the Ministry of Ayush or the State Licensing Authority (SLA) under the provisions of the Drugs and Cosmetics Act, 1940 and the Drugs and Cosmetics Rules, 1945. It authorises manufacturers, traders, and distributors to produce or sell products belonging to the Ayurvedic, Unani, Siddha, Sowa-Rigpa, and Homeopathic (AYUSH) systems of medicine. Manufacturing licences (Form 24D for Ayurveda/Unani/Siddha, Form 26E for Homeopathy) require Good Manufacturing Practices (GMP) compliance under Schedule T of the Drugs and Cosmetics Rules. The Ministry of Ayush has significantly strengthened quality enforcement in recent years — all Ayush manufacturers must comply with GMP norms, maintain batch records, and pass regular inspections. The booming demand for herbal products, nutraceuticals, and traditional medicine globally makes this a high-growth segment requiring careful regulatory compliance.
Types of Ayush Licences
Ayurvedic / Unani / Siddha Manufacturing (Form 24D):
For manufacturers producing classical and proprietary Ayurvedic, Unani, or Siddha formulations. Requires GMP-compliant facility, qualified technical head (BAMS/BUMS/BSMS degree), and dedicated quality control lab.
Homeopathic Manufacturing (Form 26E):
For manufacturers of Homeopathic medicines and mother tinctures. Requires separate facility with dilution equipment, dispensing area, and qualified Homeopathic practitioner (BHMS degree) as technical head.
Loan Licence (Form 24F):
For manufacturers without own premises who produce Ayush products using another licenced manufacturer's facility and equipment. Useful for startups launching new Ayush brands before establishing own manufacturing.
Wholesale / Retail Trading Licence:
For distributors and retailers of Ayush products. Less stringent than manufacturing — requires storage premises, qualified person, and no GMP requirement. Issued by State Drug Authority.
GMP Requirements under Schedule T
Manufacturing Premises
Separate areas for raw material receipt, weighing, manufacturing, packaging, QC lab, and finished goods storage. Temperature and humidity controlled.
Quality Control Lab
Equipped with standard analytical instruments — UV spectrophotometer, HPLC (for export products), microscope, and wet chemistry equipment. Qualified analyst on staff.
Water System
Purified water system (distillation or RO) for manufacturing. Regular testing and documentation of water quality parameters.
Documentation
Batch Manufacturing Records (BMRs), Standard Operating Procedures (SOPs), specifications for all raw materials and finished products, stability study protocols.
Personnel
Technical head with relevant Ayush degree, production manager, quality control manager. Separate persons required for production and QC.
Documents Required
Manufacturing Licence
Incorporation/partnership documents, PAN, GST, facility ownership/lease deed, detailed floor plan (production, QC lab, storage areas), equipment list, GMP documentation, Pollution Control Board certificate, technical head qualification certificates
Technical Staff
Degree certificates of technical head (BAMS/BUMS/BSMS/BHMS), experience certificates, government registration (state council), appointment letter, joining declaration
Product Documents
Product formulations with ingredient specifications, raw material sourcing certificates, batch manufacturing records format, product label specimens, shelf-life study data
Trading / Wholesale Licence
Business registration, premises proof with storage layout, qualified person's credentials, product category list, cold storage details (if applicable)
Document Type
Details
Incorporation/partnership documents, PAN, GST, facility ownership/lease deed, detailed floor plan (production, QC lab, storage areas), equipment list, GMP documentation, Pollution Control Board certificate, technical head qualification certificates
Degree certificates of technical head (BAMS/BUMS/BSMS/BHMS), experience certificates, government registration (state council), appointment letter, joining declaration
Product formulations with ingredient specifications, raw material sourcing certificates, batch manufacturing records format, product label specimens, shelf-life study data
Business registration, premises proof with storage layout, qualified person's credentials, product category list, cold storage details (if applicable)
What We Handle for You
Pre-application GMP gap assessment — identify facility and documentation gaps before filing
Determine correct licence form (24D / 26E / 24F) and category
Prepare complete application package — facility layouts, equipment list, product formulations
Technical head qualification verification and documentation
GMP documentation setup — SOPs, BMRs, specification sheets, batch records
State Licensing Authority application filing and follow-up
Inspection coordination and on-site support during SLA inspector visit
Deficiency response, compliance reporting, and re-inspection management
Amendment applications for adding new products post-licence issuance
How It Works
Share Your Details
Fill a short form or call us. We collect your requirements and all documents online — no physical visit needed.
Expert Assignment
A dedicated specialist with expertise in your service category is assigned to your case within 24 hours of payment.
Work in Progress
Your expert prepares documents, files applications with the relevant authority, and follows up on your behalf.
Delivery
Your registration certificate, legal document, or filed return is delivered digitally to your Golden Verdict dashboard.
Get Your Ayush Licence Without Any Hassle
Manufacturing and trading licence applications, GMP readiness guidance, State Licensing Authority inspection — all handled.
Pricing
Custom Quote
Pricing tailored to your specific requirements
Get Your Ayush Licence Without Any Hassle
Manufacturing and trading licence applications, GMP readiness guidance, State Licensing Authority inspection — all handled.
Pricing
Custom Quote
Pricing tailored to your specific requirements
Why Golden Verdict For
Ayush Licence?
Ayush licensing is among the most documentation-intensive processes in Indian regulatory compliance. It requires facility layout design, technical staff qualification verification, GMP readiness, raw material sourcing documentation, product formulation records, and mandatory state-level inspections. Golden Verdict has deep expertise in Ayush regulatory requirements — we conduct a pre-application GMP gap assessment, prepare the complete application package, guide facility setup to meet Schedule T requirements, manage the State Licensing Authority inspection, and deliver the licence with minimum back-and-forth.
India's Ayush revolution, fully compliant — Golden Verdict gets your licence approved.
Frequently Asked Questions
Which products require an Ayush Licence?+
Is GMP mandatory for Ayush manufacturing?+
Can I manufacture both Ayurvedic and Homeopathic products under one licence?+
What is the difference between a manufacturing licence and a trading/distribution licence?+
What happens if I want to add new products to an existing Ayush licence?+
Ready to get your Ayush Licence?
An Ayush Licence issued under the Drugs and Cosmetics Act, 1940 is mandatory for manufacturing, distributing, and selling Ayurvedic, Unani, Siddha, and Homeopathic products in India. We manage the complete State Licensing Authority application, GMP compliance, and inspection coordination.
“India's Ayush revolution, fully compliant — Golden Verdict gets your licence approved.”
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