Infrastructure built for auditable Ayurvedic production
Our facility operates under documented SOPs with full batch traceability and third-party audit access. Partners receive production capacity data and lead-time commitments before signing.
Raw Material Testing
Every incoming herbal input is tested for identity, potency, and microbial load before it enters the production line.
Tested at every stage of production
In-Process Checks
Granulation, encapsulation, and filling stages each carry documented checkpoint records tied to the batch number.
Raw material identity and potency testing on intake. In-process checks at each production stage. Finished-batch release only after full compliance sign-off.
Finished-Batch Release
No batch ships without a Certificate of Analysis and QC manager sign-off. Full traceability records available on request.
Certified, auditable, and compliant by default
WHO-GMP
AYUSH Approved
Third-Party Audit Access
World Health Organization Good Manufacturing Practice certification. Facility meets international export and domestic regulatory requirements.
Licensed under India's Ministry of AYUSH. All formulations comply with Ayurvedic Pharmacopoeia of India standards and state drug authority requirements.
Partners and their appointed auditors may inspect the facility, review batch records, and verify SOP documentation before production commitments.
Audit requests are acknowledged within one business day. Facility visits scheduled by appointment with full documentation access.