Shakumbhri Groups is a leading third-party manufacturer of nutraceuticals, Ayurvedic medicines, herbal extracts, and dietary supplements based in Khandwa, Madhya Pradesh, India. We operate under Om Shakamberi Herbals Pvt. Ltd. and Inovatiq Naturals Pvt. Ltd.

With WHO-GMP, ISO 22000, FSSAI, and US FDA certifications, we serve domestic and international clients with end-to-end manufacturing solutions — from formulation development and R&D to packaging and regulatory compliance.

We manufacture a comprehensive range of dosage forms across multiple categories:

• Tablets — Film-coated, enteric-coated, sustained-release, and effervescent tablets
• Capsules — Gelatin and HPMC vegetable-based hard capsules, soft gel capsules
• Syrups — Pediatric and adult liquid oral formulations with precise dosing
• Powders — Sachets, bulk powders, and reconstitution formulations
• Juices — Nutraceutical and therapeutic juice concentrates
• Sachets — Single-unit dose packaging for portability and convenience
• Premium Range — Advanced formulations with rare botanical extracts and specialized delivery systems

We also produce herbal extracts, essential oils, fruit powders, vegetable powders, and cosmetics.

Our primary manufacturing facility is located at:

Plot No. 7, Industrial Area, Indore Road, Khandwa — 450001, Madhya Pradesh, India.

The facility is a WHO-GMP compliant, unidirectional flow design with ISO Class 8 cleanrooms, real-time environmental monitoring, and validated cleaning protocols for multi-product suites. We maintain unidirectional material and personnel flow to prevent cross-contamination.

We maintain the highest international standards with the following certifications:

• WHO-GMP (Certificate No. WAQ25091703) — Valid till 16-09-2028
• ISO 22000:2005 (Certificate No. 17IFAU99) — Valid till 28-08-2027
• FSSAI Central License (No. 10924999000117) — Valid till 22-03-2027
• US FDA Facility Registration (No. 12421917160) — Valid till 31-12-2026

All certificates are available for download and verification on our website. Our documentation trail is audit-ready within 48 hours.

Our MOQ varies by product type and formulation complexity. As a general guideline:

• Tablets & Capsules: 10,000 to 50,000 units per SKU
• Syrups & Juices: 500 to 2,000 liters per batch
• Powders & Sachets: 100 to 500 kg per batch

We are flexible for startups and D2C brands — we have accepted pilot runs as low as 500 units for new partners. Our team works with you to find the most cost-effective batch size for your business stage.

Yes, we export to multiple countries worldwide. Our US FDA facility registration enables us to manufacture and export dietary supplements, proteins, and nutraceuticals to the United States.

We currently serve clients across:

• United States
• United Kingdom
• Europe
• Middle East
• Southeast Asia
• Africa

We provide complete export documentation including COAs, stability data, free sale certificates, and regulatory compliance packages tailored to destination country requirements.

Yes, we specialize in both private label and custom formulation manufacturing.

Our in-house R&D team includes qualified pharmacists, phytochemists, and formulation scientists who can:

• Develop custom formulations from scratch based on your target ingredients and health claims
• Optimize existing formulations for bioavailability, stability, and taste
• Provide private label manufacturing with your branding on our proven formulations
• Conduct accelerated stability testing (40°C/75% RH) and shelf-life studies
• Perform HPTLC fingerprinting and dissolution profile matching

We work through multiple iterations until your formulation meets exact specifications — one client went through 11 iterations to perfect their plant-based capsule shell integrity.

Quality is embedded in every stage of our manufacturing process:

• Raw Material Testing: Every incoming batch is tested for identity, purity, potency, and contaminants
• In-Process Controls: Real-time monitoring of weight variation, hardness, friability, and disintegration
• Finished Product Testing: Full microbiological, chemical, and physical parameter verification
• Environmental Monitoring: ISO Class 8 cleanroom with continuous particulate and microbial monitoring
• Documentation: Batch manufacturing records, SOPs, and change control logs maintained per WHO-GMP

Over three consecutive years and 847 batches, our partners recorded exactly zero quality defects. Our customer complaint rate dropped client complaints from 12% to 0.3% within six months.

Timelines depend on formulation complexity and raw material availability. Typical lead times are:

• Existing Formulations (Private Label): 2 to 4 weeks from order confirmation
• New Custom Formulations: 4 to 8 weeks including R&D and pilot batch approval
• Export Orders: Add 1 to 2 weeks for documentation and regulatory packaging compliance

We maintain a robust supply chain with secondary cold-chain partners to ensure on-time delivery even during disruptions. During the 2024 monsoon, we rerouted shipments and delivered two days ahead of schedule.

We offer comprehensive packaging solutions to match your brand positioning:

• Primary Packaging: Blister packs, Alu-Alu packs, strip packs, bottles (HDPE/PET), jars, and sachets
• Secondary Packaging: Cartons, labels, inserts, and tamper-evident seals
• Tertiary Packaging: Shipper boxes, palletization, and export-ready packaging
• Custom Branding: Your logo, brand colors, and regulatory label design support

We can accommodate eco-friendly and sustainable packaging options including biodegradable materials and recycled content upon request.

Absolutely. Regulatory compliance is one of our core strengths. We provide:

• Product Dossiers: Complete technical documentation for regulatory submissions
• Stability Data: Accelerated and real-time stability studies with comprehensive reports
• Certificate of Analysis (COA): Batch-specific testing results for every production lot
• Free Sale Certificates and Manufacturing Licenses for export markets
• Label Compliance Review: Ensuring your labels meet FSSAI, FDA, and EU regulatory requirements
• Quarterly Business Reviews: SKU-level Pareto analysis and regulatory update briefings

Our documentation trail is audit-ready within 48 hours — a level of predictability that our partners find invaluable.

Yes, we actively support startups, D2C brands, and emerging wellness companies. We understand that every large brand started small.

Our startup-friendly services include:

• Low MOQ pilot runs to test market response before scaling
• Dedicated formulation scientist assigned to your project
• Flexible payment terms for qualifying new partners
• Brand development support including packaging design guidance
• Scalable manufacturing — grow from 500 units to 100,000+ units monthly without switching manufacturers

One D2C brand partner scaled from 500-unit pilot runs to over 100,000 units monthly across 14 SKUs while maintaining zero quality recalls.

We source and work with a wide spectrum of high-quality raw materials:

• Ayurvedic Herbs: Ashwagandha, Safed Musli, Shatavari, Gokshura, Arjuna, Tulsi, Curcumin, and 100+ traditional botanicals
• Nutraceutical Actives: Glutathione, L-Carnitine, Omega-3 fatty acids, CoQ10, Melatonin, and specialized amino acids
• Vitamins & Minerals: Complete range of USP/EP-grade vitamins and chelated minerals
• Proteins: Whey protein, plant proteins, collagen peptides, and hydrolyzed variants
• Excipients: HPMC, gelatin, maize starch, magnesium stearate, and pharma-grade carriers

All raw materials are sourced from certified vendors with full traceability. We maintain COAs and vendor qualification records for every ingredient.

Getting started is simple and transparent:

• Step 1: Share your product concept, target formulation, or reference product
• Step 2: We provide a detailed quotation with MOQ, timeline, and pricing
• Step 3: Our R&D team develops samples or pilot batches for your approval
• Step 4: Upon approval, we proceed to commercial production with full QC documentation
• Step 5: Your products are delivered with complete regulatory documentation

We offer free initial consultations and formulation feasibility assessments. Our typical response time for quotations is within 24 to 48 hours.