Ayurvedic & Nutraceutical Third Party Manufacturing Company India

Ayurvedic & Nutraceutical Export Manufacturer India | WHO-GMP Contract Manufacturing | Shakumbhri Groups
Shakumbhri Groups  ·  Khandwa, Madhya Pradesh, India

Ayurvedic & Nutraceutical
manufacturing, built for export.

WHO-GMP, ISO 22000 and US FDA registered contract manufacturing — with in-house R&D, private label services, and complete export documentation for brand owners shipping to 50+ countries.

WHO-GMP CERTIFIED ISO 22000 US FDA REGISTERED AYUSH · FSSAI · NABL HALAL · KOSHER
200+Brands Served
20+Countries Exported To
15+Years in Operation
847Batches, Zero Defects*
500+Formulas Developed
200+Brands Served
50KSq Ft Facility
15+Years Experience
100+Team Members
20+Countries Served
5M+Units Produced
End-to-end, under one roof

Six services. One accountable partner.

From first formulation brief to a container leaving Khandwa — every step happens inside the same WHO-GMP facility, with one team you can call.

01

Third Party Manufacturing

Complete contract manufacturing — from raw material sourcing to finished, packed goods — at our WHO-GMP certified facility.

WHO-GMPAYUSHBulk Orders
02

Private Label Services

Launch your own Ayurvedic or nutraceutical brand fast — ready-to-market products with your branding, labels, and export-ready packaging.

Custom BrandingLow MOQ30-Day Launch
03

R&D & Custom Formulation

In-house scientists blend Ayurvedic wisdom with modern science to create proprietary, market-ready formulations for your brand.

Herbal ExtractsTablets & CapsulesSyrups
04

Export & Compliance

Complete documentation, regulatory compliance, and shipping support for hassle-free entry into 50+ global markets.

US FDA ReadyEU CompliantHalal/Kosher
05

Quality & Certification

Rigorous batch testing across WHO-GMP, ISO 22000, FSSAI, AYUSH and NABL accredited facilities, with a zero-defect track record.

ISO 22000NABLOrganic Certified
06

Premium Packaging & Dispatch

Air-tight, UV-protected primary and secondary packaging with a final quality audit before secure, on-time dispatch.

Custom PackagingExport-ReadyOn-Time Dispatch
Research & development

Formulation science behind every batch.

Our R&D team doesn’t just replicate existing products — it builds and stress-tests formulations until they hold up in your target market’s climate, shelf life, and regulatory review.

15+R&D Scientists
50+New Formulas / Year
100%Customizable
Market feasibility & ingredient selectionWe align with your brand vision, run feasibility studies, and identify key actives before formulation starts.
Bioavailability & stability optimizationFormulations are refined for absorption, taste, and shelf stability under real-world storage conditions.
Accelerated stability testingBatches are tested at 40°C/75% RH to validate shelf-life claims before commercial production.
HPTLC fingerprinting & dissolution matchingEvery formulation is fingerprinted and profile-matched for batch-to-batch consistency.
Iterative refinementWe work through as many formulation rounds as it takes — one partner went through 11 iterations to perfect a capsule shell.
Manufacturing capabilities

Every dosage form, one facility.

Tablets

Film-coated, enteric-coated, sustained-release and effervescent tablets with controlled-release mechanisms.

Capsules

Gelatin and HPMC vegetable-based hard capsules, plus soft gel capsules for sensitive actives.

Syrups

Palatable liquid formulations with precise dosing, suited for pediatric and geriatric use.

Powders & Sachets

Bulk powders, reconstitution formulations, and single-dose sachets for portability and shelf-life.

Juices

Nutraceutical and therapeutic juice concentrates fortified with vitamins, minerals and herbal extracts.

Oils & Ointments

Ayurvedic oils, balms and topical formulations manufactured under the same quality controls.

Herbal Extracts

Standardized, high-potency extracts manufactured in-house for consistent raw material quality.

Premium Range

Advanced formulations with rare botanicals and specialized delivery systems for premium positioning.

Certified & audit-ready

Documentation your compliance team won’t have to chase.

WHO-GMP

CERT NO. WAQ25091703
VALID TILL 16-09-2028

ISO 22000

CERT NO. 17IFAU99
VALID TILL 28-08-2027

FSSAI Central License

LIC. NO. 10924999000117
VALID TILL 22-03-2027

US FDA Registered

REG. NO. 12421917160
VALID TILL 31-12-2026

AYUSH Certified

Ministry of AYUSH approved facility for Ayurvedic & herbal manufacturing.

NABL Accredited Lab

In-house analytical testing for reliable, accurate batch results.

Halal Certified

Compliant distribution for GCC & Southeast Asian markets.

Kosher Certified

Enabling compliant distribution to specialized global markets.

Facility: Plot No. 7, Industrial Area, Indore Road, Khandwa – 450001, Madhya Pradesh. A WHO-GMP compliant, unidirectional-flow facility with ISO Class 8 cleanrooms, real-time environmental monitoring, and validated cleaning protocols across our multi-product lines. Facility visits and audits are welcomed before you commit to an order.
Global reach

Export-ready from day one.

Our US FDA registered facility ships to brand owners and distributors across 20+ countries, with every document your customs broker or regulatory reviewer will ask for.

🇺🇸 United States 🇬🇧 United Kingdom 🇪🇺 Europe 🇦🇪 Middle East 🌏 Southeast Asia 🌍 Africa
Documentation included
Certificate of Analysis (COA)Batch-specific
Stability DataAccelerated + real-time
Free Sale CertificatePer destination market
Product DossierFor regulatory submission
Label Compliance ReviewFSSAI / FDA / EU
Audit TurnaroundWithin 48 hours
Detailed workflow overview

From your brief to a dispatched container.

01

Plan & R&D

We align with your brand vision, run market feasibility studies, and identify key ingredients and safety benchmarks.

02

Custom Formulation

Scientists build your product profile, balancing traditional efficacy with shelf-stability and regulatory needs.

03

Ingredient Sourcing

Vetted global suppliers provide high-potency botanicals; each batch is purity-tested before production.

04

Production

Pilot-scale to mass-production machinery blends and processes ingredients in a controlled, sterile environment.

05

Premium Packaging

Primary and secondary packaging focused on air-tight integrity, UV protection, and your brand presentation.

06

Final Dispatch

A last quality audit, complete documentation, secure crating, and logistics to your warehouse or freight forwarder.

Verified partner testimonials

Trusted by 200+ brands across 20+ countries.

★★★★★

“We scaled from 10,000 to over 100,000 units monthly across 14 SKUs without a single quality recall. Their HPTLC fingerprinting and dissolution profile matching stands out in the industry.”

Founder & CEO, Nutraceutical Brand Partner · Third-Party Manufacturing
★★★★★

“Their capsule line passed accelerated stability testing at 40°C/75% RH for 24 months with zero degradation — true mastery of Ayurvedic extraction and modern phytopharmaceutical science.”

Director of R&D, Wellness Nutraceutical Partner
★★★★★

“Over three years and 847 batches across our portfolio, we recorded exactly zero quality defects. Their documentation trail is audit-ready within 48 hours.”

Operations Head, Multi-Product Manufacturing Partner
★★★★★

“When 2024 monsoon disruptions hit road freight, their team rerouted our shipment through a secondary cold-chain partner — we received our consignment two days ahead of schedule.”

CEO, Export Supply Chain Partner

The Startup “Glow-Up”

A boutique wellness startup struggled with complex regulations. We handled their R&D and entire compliance lifecycle.

Result: 10,000+ units sold in Q1 nationwide

Scaling Through Demand

A regional brand faced an “out of stock” crisis. We overhauled their production lines to meet a 5x increase in demand.

Result: 99.8% product availability achieved

The Global Leap

An Ayurvedic brand wanted to export but couldn’t meet international purity standards. We upgraded their supply chain.

Result: Successful entry into the European market
Frequently asked questions

Everything brand owners ask before exporting.

Who is Shakumbhri Groups?

Shakumbhri Groups is a third-party manufacturer of nutraceuticals, Ayurvedic medicines, herbal extracts, and dietary supplements based in Khandwa, Madhya Pradesh, India, operating under Om Shakamberi Herbals Pvt. Ltd. and Inovatiq Naturals Pvt. Ltd. It holds WHO-GMP, ISO 22000, FSSAI, and US FDA certifications and serves domestic and international clients with end-to-end manufacturing solutions.

What products does Shakumbhri Groups manufacture?

Tablets, capsules, syrups, powders, juices, sachets, and a premium range with advanced delivery systems, plus herbal extracts, essential oils, fruit and vegetable powders, and cosmetics.

Where is the manufacturing facility located?

Plot No. 7, Industrial Area, Indore Road, Khandwa – 450001, Madhya Pradesh, India — a WHO-GMP compliant, unidirectional-flow facility with ISO Class 8 cleanrooms, also registered with the US FDA (No. 12421917160) for export to the United States.

What certifications does Shakumbhri Groups hold?

WHO-GMP (Cert. No. WAQ25091703, valid till 16-09-2028), ISO 22000 (Cert. No. 17IFAU99, valid till 28-08-2027), FSSAI Central License (No. 10924999000117, valid till 22-03-2027), and US FDA Facility Registration (No. 12421917160, valid till 31-12-2026).

What is the minimum order quantity (MOQ)?

Tablets & Capsules: 10,000–50,000 units per SKU. Syrups & Juices: 500–2,000 liters per batch. Powders & Sachets: 100–500 kg per batch. Pilot runs as low as 500 units are accepted for new brand partners.

Does Shakumbhri Groups export internationally?

Yes — to the United States, United Kingdom, Europe, Middle East, Southeast Asia, and Africa, backed by complete COAs, stability data, free sale certificates, and destination-specific regulatory packages.

Does Shakumbhri Groups offer private label and custom formulation services?

Yes. The in-house R&D team of pharmacists, phytochemists and formulation scientists develops custom formulations from scratch, optimizes existing ones for bioavailability and stability, and offers private label manufacturing on proven formulations — including accelerated stability testing and HPTLC fingerprinting.

What quality control measures are followed?

Raw material identity/purity testing, in-process controls (weight variation, hardness, disintegration), full finished-product microbiological and chemical testing, ISO Class 8 cleanroom environmental monitoring, and complete batch documentation per WHO-GMP.

What is the typical production timeline?

Existing formulations for private label: 2–4 weeks from order confirmation. New custom formulations: 4–8 weeks including R&D and pilot batch approval. Export orders add 1–2 weeks for documentation.

What packaging options are available?

Primary: blister packs, Alu-Alu packs, strip packs, bottles, jars, sachets. Secondary: cartons, labels, tamper-evident seals. Tertiary: export-ready shipper boxes and palletization, with custom branding and eco-friendly options on request.

Can Shakumbhri Groups help with regulatory compliance and export documentation?

Yes — product dossiers, stability data, batch-specific Certificates of Analysis, free sale certificates, manufacturing licenses, and label compliance review for FSSAI, FDA and EU markets, with an audit-ready documentation trail within 48 hours.

Does Shakumbhri Groups work with startups and small brands?

Yes — low-MOQ pilot runs, a dedicated formulation scientist per project, and scalable manufacturing from 500-unit pilots to 100,000+ units monthly on the same production line, without switching manufacturers.

What raw materials does Shakumbhri Groups source?

Ayurvedic herbs (Ashwagandha, Safed Musli, Shatavari, Curcumin and 100+ botanicals), nutraceutical actives (Glutathione, L-Carnitine, Omega-3, CoQ10), USP/EP-grade vitamins and minerals, proteins (whey, plant, collagen peptides), and pharma-grade excipients — all from certified, traceable vendors.

How do I get started with Shakumbhri Groups?

Share your product concept or reference product → receive a detailed quotation with MOQ, timeline and pricing → approve an R&D sample or pilot batch → move to commercial production with full QC documentation → receive your goods with complete export paperwork. Typical quotation response time is 24–48 hours.

Get your free manufacturing plan

Let’s scope your export line.

Tell us what you want manufactured and where it’s shipping. A manufacturing consultant responds — typically within 5 minutes during business hours.

1
Free feasibility assessmentNo cost, no commitment — just a straight answer on whether it’s buildable.
2
Quotation within 24–48 hoursMOQ, pricing, and timeline in writing before you commit.
3
Dedicated formulation scientistOne point of contact from R&D sample through to dispatch.
🔒 Secure & confidential · ⚡ Reply in ~5 min · ✅ WHO-GMP certified
Ready when you are

Let’s build your
export-ready brand.

Talk to a manufacturing consultant directly — no forms required.

📞 +91 95222 36162 Plot No. 7, Industrial Area, Indore Road, Khandwa – 450001, MP
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