Export-Grade Third Party Nutraceutical Manufacturing
Manufacturing Capabilities
Capsules
- Vegan
- Gelatine
- 0 (zero), 00 (double-zero) size
- Colour & branding
Tablets
- Coated
- Un-coated
- Chewable
- Effervescent
Softgels
- Fat-Soluble Vitamins
- Omega-3
- Fish oil
Powders
- Powdered blends
- Energy electrolyte powders
- Functional drink mixes
Liquids
- Vitamin tonics
- Herbal syrups
- Drops
Next Gen Formats
- Honey-gels
- Shots
- Gummies (coming soon)
Global Compliance and Quality Assurance
HimPharm operates under internationally recognised regulatory and quality frameworks to ensure consistent, export-ready nutraceutical manufacturing across global markets.
WHO-GMP Certified
Manufacturing facilities and production systems comply with World Health Organization Good Manufacturing Practices, ensuring controlled processes, batch traceability, and consistent product quality at scale.Manufacturing facilities and production systems comply with World Health Organization Good Manufacturing Practices, ensuring controlled processes, batch traceability, and consistent product quality at scale.
ISO 9001:2015 Certified
Implementation of a structured quality management system covering procurement, production, quality control, documentation, and customer satisfaction, supporting repeatable outcomes and process reliability.
Halal Certified
Halal certification in accordance with Islamic regulatory requirements, enabling compliant exports to GCC, Middle East, and other Muslim-majority markets.
FSSAI Licensed
Licensed by the Food Safety and Standards Authority of India for nutraceutical and food-grade manufacturing, ensuring compliance with Indian regulatory requirements for domestic and export supply.
US FDA Food Facility Registered
Registered with the United States Food and Drug Administration as a food facility, validating hygiene controls, food safety systems, and readiness for US import procedures.
In addition to certifications, HimPharm provides complete export and regulatory documentation support, including Certificates of Analysis (CoA), MSDS, Free Sale Certificates, and shipment documentation, enabling smoother customs clearance and regulatory acceptance across the US, Europe, MENA, Africa, and other regulated markets.
Manufacturing Facilities and Capacity
Integrated Manufacturing Infrastructure
- Dedicated nutraceutical manufacturing blocks segregated by dosage form
- Controlled material and personnel flow aligned with WHO-GMP requirements
- Separate zones for blending, compression, filling, and packing
- Quarantine, approved, and rejected material storage areas
Dosage Form Capabilities
- Capsules, vegetarian and gelatin, single-active and complex blends
- Tablets, coated and uncoated nutraceutical formulations
- Powders and sachets for functional and specialty blends
- Liquids and syrups including drops, tonics, and liquid supplements
Production Scale & Batch Flexibility
- Pilot batches for new product development and market testing
- Commercial-scale manufacturing for established brands
- Flexible batch sizes to support multiple SKUs simultaneously
- Capacity planning designed to protect lead times during scale-up
In-House Quality Control & Testing
- On-site quality control laboratories
- Raw material identity and compliance verification
- In-process quality monitoring during manufacturing
- Batch-wise finished product testing and release
Packaging & Dispatch Readiness
- In-house packing for bottles, jars, capsules, and sachets
- Export-grade secondary and tertiary packing standards
- Palletised, container-ready dispatch formats
- Experience handling both air and sea freight consignments
Export-Oriented Facility Design
- Facilities structured for regulated and semi-regulated markets
- Experience supplying the US, Europe, Middle East, Africa, and Asia
- Documentation and traceability systems
- Designed for repeat commercial supply and long-term contracts
Custom Formulation, Private Label and White Label
HimPharm supports nutraceutical brands at different stages of scale, from early-stage product development to full-scale private label and ready-to-ship white label solutions. Clients can engage at the level that best matches their commercial and regulatory requirements.
Custom Formulation & R&D
We develop new nutraceutical formulations and improve or replicate existing reference products to meet specific market, dosage, and regulatory objectives.
- Custom formulation development based on target claims, dosage form, and intended market
- Ability to match or optimise reference products while maintaining regulatory compliance
- Active ingredient sourcing from approved suppliers with defined quality specifications
- Consideration of stability, bioavailability, compatibility, and shelf life during formulation
- Support for flavour development and sensory optimisation where applicable
This route is typically chosen by brands seeking product differentiation, proprietary blends, or market-specific customisation.
Private Label Manufacturing
Private label manufacturing is suited for brands that bring a product concept or positioning and require a complete manufacturing and packaging partner.
- End-to-end support covering formulation, manufacturing, packing, and documentation
- Assistance with label content alignment to regulatory requirements of target markets
- Multiple dosage forms and packaging formats under a single manufacturing partner
- Scalable production suitable for both new launches and ongoing commercial supply
This model allows brands to retain ownership of positioning and branding while outsourcing operational complexity.
White Label Ready Products
White label solutions are designed for faster market entry with reduced development timelines and lower entry barriers.
- Ready, tested nutraceutical formulations with fixed specifications
- Standardised pack sizes and dosage formats
- Lower minimum order quantities compared to custom or private label routes
- Suitable for distributors, new brands, and market testing
White label products enable rapid launches while maintaining manufacturing and compliance standards.
MOQs, Lead Times and Commercial Terms
HimPharm follows a structured engagement model designed to support both new product launches and scalable commercial supply, while maintaining quality, compliance, and delivery reliability.
Minimum Order Quantities (MOQs)
Minimum order quantities vary based on product type, formulation complexity, packaging format, and regulatory requirements.
- White Label Products
Lower entry MOQs with predefined formulations and pack sizes, suitable for faster market entry. - Private Label Products
Moderate MOQs aligned to commercial manufacturing efficiencies and packaging configurations. - Custom Formulation Projects
MOQs determined after formulation finalisation, stability considerations, and batch-size feasibility.
Exact MOQs are confirmed during technical and commercial evaluation to ensure production efficiency and consistent quality.
Lead Times
Lead times depend on formulation route, artwork readiness, and order type.
- New Product Development and Sampling
Typically includes formulation development, sample preparation, and approval prior to commercial production. - First Commercial Production
Lead time begins after final formula approval, packaging artwork sign-off, and receipt of advance payment. - Repeat Orders
Shorter and more predictable lead times, subject to raw material availability and production scheduling.
Indicative timelines are shared during project evaluation and confirmed at order placement.
Commercial Terms and Engagement Model
Commercial terms are structured to balance transparency, operational planning, and long-term supply stability.
- Pricing is driven by formulation composition, raw material costs, batch size, packaging format, and compliance requirements
- Advance payment is typically required to initiate production, with balance terms aligned to dispatch or documentation milestones
- Manufacturing is executed against approved specifications and signed commercial agreements
- Intellectual property, confidentiality, and formula ownership are addressed contractually
HimPharm supports both one-time projects and long-term manufacturing partnerships, depending on client requirements.
Documentation & Export Support
HimPharm provides complete technical, regulatory, and commercial documentation required for domestic and international nutraceutical supply.
Quality & Regulatory Documentation
- Certificate of Analysis (CoA) for finished products
- Raw material compliance documentation where applicable
- MSDS / Safety Data Sheets
- Manufacturing and quality certifications as required
Export & Commercial Documentation
- Commercial invoice and packing list
- Certificate of Origin and Free Sale Certificate (where applicable)
- Export packing and palletisation documentation
- Support for client-nominated or HimPharm-managed logistics
Market & Compliance Support
- Documentation aligned to requirements of the US, Europe, Middle East, Africa, and Asia
- Experience supporting regulated and semi-regulated markets
- Label and pack review support for market compatibility
Documentation sets are prepared based on product type, destination market, and regulatory pathway, and are finalised prior to dispatch to support smoother customs clearance and downstream registration processes.
Share Your Product Brief
For an Indicative MOQs, Timelines, and Pricing fill out the form and share your product brief.
These statements have not been evaluated by the Food and Drug Administration. These products are not intended to diagnose, treat, cure, or prevent any disease.
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