End-to-end Ayurvedic and nutraceutical manufacturing for global brands. Custom formulation, private label, or white label — delivered with FSSAI, AYUSH, GMP, and ISO discipline. In as little as four weeks.
We handle every stage of bringing your wellness product to market — from the moment you describe what you want to the day it lands on your buyer's shelf.
Unlike most contract manufacturers, we don't outsource sourcing to brokers, QC to third parties, or regulatory to consultants. It's all in one facility. One accountable team. One COA per batch.
Pick the bundle you need. Most partners use all six; some use only what their internal team can't deliver in-house.
From a single-line brief to a finalized, stable, market-ready formula — including bioavailability optimization and palatability tuning.
Direct relationships with Ayurvedic herb growers, Himalayan resin suppliers, and Korean botanical extract houses — no middlemen.
Five production lines covering capsules (gelatin/vegan), tablets, powders, effervescents, gummies, and topical formats.
In-house analytical lab with HPLC, GC-MS, HPTLC, and microbiology — no third-party delays, no surprises.
Primary and secondary packaging in your brand's design — or use our standard catalog for faster turnaround.
End-to-end paperwork for your launch market — FSSAI, AYUSH, FDA, FSSC 22000, plus Halal/Kosher certification support.
Total timeline: 4–12 weeks depending on formulation complexity and regulatory needs.
You submit an RFQ. Within 48 hours, our team schedules a video call to understand your vision, target market, regulatory needs, and timeline. We sign a mutual NDA if requested.
Our R&D team proposes a formula (or refines yours), our QC head signs off on technical feasibility, and you receive a complete written proposal with per-unit pricing across MOQ tiers.
We prepare physical samples in your specified dosage form. You taste, test, and request adjustments. Each adjustment cycle takes 3–5 days. Most partners settle the formula in 2 rounds.
Once samples are approved, you sign the manufacturing agreement. We require 50% advance to begin raw material procurement; balance due before dispatch.
Raw materials arrive, identity testing confirms purity, production runs on dedicated lines, and our in-house QC lab tests every batch against your specifications. You receive a Certificate of Analysis.
Your primary and secondary packaging is applied. Final inspection covers labeling accuracy, batch coding, packaging integrity, and quantity verification.
We dispatch to your warehouse or freight forwarder with complete documentation: invoice, packing list, COA, Free Sale Certificate, and any market-specific paperwork required.
All production runs on calibrated cGMP equipment in our Faridabad facility. Detailed equipment list available under NDA.
| Dosage Form | Capacity (per day) | Minimum Order | Lead Time |
|---|---|---|---|
| Hard Gelatin / Vegan Capsules CAPSULES |
120,000 units | 5,000 units | 4–6 weeks |
| Compressed Tablets TABLETS |
200,000 units | 10,000 units | 4–6 weeks |
| Powders & Granules (sachets/jars) POWDERS |
800 kg | 500 kg or 5,000 sachets | 4–5 weeks |
| Effervescent Tablets EFFERVESCENT |
80,000 units | 10,000 units | 5–7 weeks |
| Syrups & Liquids LIQUIDS |
2,000 litres | 500 litres | 4–6 weeks |
| Topicals (creams, oils) TOPICAL |
500 kg | 200 kg | 5–6 weeks |
| Gummies (pectin-based) GUMMIES |
60,000 units | 15,000 units | 6–8 weeks |
Audited, renewed, and verifiable. Soft copies available on request; originals on display at our facility.
They gave us samples in 11 days. Korean regulatory in 6 weeks. First batch on shelf in 10. No supplier in our network could match that — and the COAs match the marketing claims, every time.
Three short steps. A custom quote in your inbox within 48 hours. No commitment, no pressure.