A Platform of Four Specialised
Manufacturing Campuses.
One Integrated Partner.
Jireh Nutrition Hub is not a single factory but a platform, It is a purpose-built network of four GMP-certified manufacturing units — each designed, certified, and staffed for a specific product category. Nutraceuticals. Pharmaceuticals. Ayurveda & Organics. Peptide Synthesis. Collectively, they house 4,700+ active SKUs, 8,700+ validated formulations, and the production depth to supply global supplement and pharma brands at any scale.
Why Four Facilities
Outperform One Large Factory
Most contract manufacturers operate a single facility and ask every product category to share the same production lines, the same cleanrooms, and the same regulatory framework. That model creates bottlenecks, cross-contamination risks, and certification conflicts. Jireh Nutrition Hub was built differently.
Each of our four manufacturing campuses is purpose-built and independently certified for its category. The nutraceutical unit does not share floor space with the pharmaceutical cleanroom. The Ayurvedic unit does not run on the same production schedule as the peptide synthesis lab. Each facility has its own GMP certification, its own quality management team, and its own dedicated equipment — sized, calibrated, and validated for the products it produces.
This architecture eliminates the compromise that haunts single-facility CDMOs. Your capsule line never waits because the tablet press is occupied. Your Ayurvedic churna is never contaminated by pharmaceutical excipient residue. Your peptide batch is never delayed by a nutraceutical production surge. Parallel capacity across four specialist campuses is the infrastructure advantage that global brands come to India for — and that Jireh has specifically built.
Four Campuses.
Four Specialisations.
Zero Compromise.
Every facility in the Jireh network is independently certified, independently staffed, and independently validated for its designated product categories. Each operates under its own quality management system, with dedicated QC laboratories, environmental monitoring protocols, and batch release procedures appropriate to its regulatory framework.
Our flagship nutraceutical production campus houses India’s most comprehensive range of solid dosage form manufacturing equipment under a single GMP-certified roof. Designed specifically to serve international supplement brands requiring export-grade nutraceuticals across all major dosage formats, this unit operates at capacity scales from low-MOQ startup runs through to high-volume commercial production. Separate granulation, compression, coating, encapsulation, and packaging suites operate independently with airlocked transfer protocols between each. Environmental monitoring for particulate count, temperature, relative humidity, and differential pressure is continuous and logged. All formulations are validated per ICH Q8 guidelines before production commences.
Our pharmaceutical production campus is engineered to the most stringent manufacturing standard in global medicine: WHO-GMP. India supplies 20% of the world’s generic medicines, and this facility is built to meet the regulatory requirements of the regulated markets that consume them — USA, EU, UK, and the Middle East. The campus features dedicated cleanroom environments classified to ISO 5 (Grade A/B) through ISO 8 (Grade D) for sterile product manufacturing. Separate production suites for oral solid dosage forms, liquid orals, sterile injectables, and semi-solid topicals ensure zero cross-contamination risk. All critical parameters — HVAC, water systems (WFI and purified water), compressed air, and environmental controls — are validated, qualified, and continuously monitored through an automated building management system.
India’s AYUSH Ministry licensing is not a cosmetic credential — it is a rigorous government-issued manufacturing authorisation that verifies a facility’s adherence to the Ayurvedic Pharmacopoeia of India and the Ayurvedic Formulary of India. Our AYUSH-licensed campus is one of relatively few facilities in India equipped to manufacture both classical Ayurvedic preparations (arishtas, asavas, avaleha, churnas) and modern standardised herbal extracts under a single regulatory umbrella. The facility houses dedicated extraction suites for water, alcohol, and CO2 supercritical extraction; spray-drying towers for powder manufacture; traditional preparation rooms for classical formulations; and a lyophilisation unit for high-value botanical extracts. USDA Organic and India Organic (NPOP) certified handling procedures apply across the organic product lines, with complete chain-of-custody documentation from certified farm to finished goods.
Advanced peptide synthesis requires a fundamentally different manufacturing environment from conventional pharmaceutical or nutraceutical production — and that is precisely why it occupies its own dedicated campus. Our GMP peptide synthesis laboratory houses automated Fmoc solid-phase peptide synthesisers, preparative HPLC purification systems with fraction collection, industrial lyophilisers, and a fully equipped analytical suite including RP-HPLC, ESI mass spectrometry, and amino acid analysis. Every synthesis is monitored in real-time through in-process coupling efficiency testing, and every batch passes full analytical release testing before dispatch. The facility operates under GMP principles aligned with ICH Q7 for active pharmaceutical ingredients, making it one of the only dedicated GMP peptide synthesis labs in India capable of supplying pharmaceutical-grade peptide APIs alongside research and commercial grade products from the same validated facility.
The Systems That Run
Across All Four Campuses
While each manufacturing unit operates independently for its category, the Jireh network shares a common backbone of infrastructure systems — utility systems, water systems, IT infrastructure, and central documentation management — that ensure consistency and reliability across all production campuses.
Dedicated water purification infrastructure per campus. Pharmaceutical campus operates Water for Injection (WFI) quality distribution loops. Nutraceutical and Ayurvedic units run validated Purified Water (PW) systems meeting USP and EP specifications. Regular conductivity, TOC, microbial, and endotoxin monitoring logs maintained.
HVAC systems across all four campuses are validated against ISO 14644 cleanroom classification standards. The pharmaceutical campus maintains ISO 5 (Grade A) conditions in sterile filling zones and Grade B background environments. Nutraceutical and Ayurvedic production areas are maintained at Grade C/D. Temperature, relative humidity, differential pressure, and particle counts are monitored continuously through integrated BMS systems with automated alerts.
Manufacturing continuity requires uninterrupted utility supply. All four campuses operate with grid power backed by captive diesel generation with automatic changeover — ensuring no production interruption during power outages. Cold storage areas, refrigerated warehouses, and lyophilisation units are connected to dedicated UPS systems with extended battery autonomy. Compressed air systems are validated and oil-free across all production areas.
End-to-end traceability from raw material receipt to finished goods dispatch is managed through our integrated enterprise resource planning system. Every batch carries a unique lot number traceable through every production step, quality test, and warehouse movement. Electronic batch manufacturing records are generated automatically and archived with restricted access, providing client-facing batch traceability reports on request.
Raw material, in-process, and finished goods warehouses are fully segregated and climate-controlled. Temperature-sensitive materials — botanical extracts, peptides, probiotics — are held in validated cold rooms with continuous temperature monitoring and alarm systems. Quarantine, approved, and rejected material areas are physically separated and access-controlled. Finished goods are held under export packaging conditions pending dispatch.
Primary packaging (bottle filling, blister sealing, vial stoppering) through to secondary packaging (carton erection, leaflet insertion, shrink wrapping) and export-ready tertiary packaging (master case packing, palletisation) are all performed in-house. Label printing, serialisation, and market-specific compliance labelling are managed through dedicated software with version control. Packaging materials are tested for compatibility and released through the same QC process as manufactured products.
A QC Lab Built for
International Release Standards
Every product manufactured at Jireh Nutrition Hub passes through our in-house quality control laboratory before release. Our QC lab is equipped to perform the full spectrum of analytical testing required for nutraceutical, pharmaceutical, Ayurvedic, and peptide products — from basic identity and potency testing to advanced chromatographic characterisation and stability studies. External NABL-accredited third-party testing is available for any batch on client request.
Instruments Behind
Every Batch Certificate
Controlled Environments
That Protect Every Batch
A GMP certificate is only as strong as the environmental controls that maintain its validity day-to-day. At Jireh, cleanroom classification, environmental monitoring, personnel gowning procedures, and airflow management are not compliance exercises — they are the operational foundation of every batch we manufacture and every CoA we issue.
Our pharmaceutical campus operates cleanroom suites across ISO 5 through ISO 8 classifications, with the most stringent Grade A/B conditions maintained in sterile product manufacturing zones. Nutraceutical production areas are maintained at Grade C/D. All environmental classification data is continuously logged, trended, and available to clients as part of facility audit documentation packages.
Monitored. Logged.
Continuously Verified.
Continuous environmental monitoring across all production areas — with automated alerts, deviation records, and trending reports available to clients during facility qualification audits.
| Parameter | Method | Frequency | Standard |
|---|---|---|---|
| Non-Viable Particulates | Laser particle counter | Continuous | ISO 14644 |
| Viable Airborne Microbes | Active air sampling | Per shift | EU GMP Annex 1 |
| Surface Microbial Count | Contact plates (RODAC) | Per campaign | USP <1116> |
| Temperature | Calibrated data loggers | Continuous | ICH Q1A |
| Relative Humidity | Calibrated data loggers | Continuous | ICH Q1A |
| Differential Pressure | Magnehelic gauges + BMS | Continuous | GMP Compliant |
| Air Change Rate | Anemometry | Semi-annual | ISO 14644-3 |
The Scale to Supply
Startups to Enterprises
Our four-campus model provides independent production capacity per category — meaning a surge in pharmaceutical demand does not delay your nutraceutical order, and a large Ayurvedic contract does not push back your peptide shipment. Each unit maintains its own production scheduling. We offer low MOQs for brand launches and scale incrementally as your demand grows — with no disruption to existing client production timelines.
Which Certifications Apply
to Your Product Category
International buyers frequently ask which certifications apply to their specific product. The answer depends on which of our four manufacturing units will produce it. This matrix maps our active certifications to each campus, so your regulatory team has the precise compliance information they need.
| Certification / Approval | Unit 01 · Nutraceuticals | Unit 02 · Pharmaceuticals | Unit 03 · Ayurveda | Unit 04 · Peptides |
|---|---|---|---|---|
| GMP (Good Manufacturing Practice) | ✓ Active | ✓ Active | ✓ Active | ✓ Active |
| ISO 9001:2015 | ✓ Organisation-Wide | ✓ Organisation-Wide | ✓ Organisation-Wide | ✓ Organisation-Wide |
| WHO-GMP | ~ Alignment | ✓ Certified | ~ Alignment | ~ Alignment |
| FSSAI License | ✓ Active | ✓ Active | ✓ Active | ~ Where Applicable |
| HACCP | ✓ Certified | ✓ Certified | ✓ Certified | ~ Where Applicable |
| AYUSH License | ✗ Not Applicable | ✗ Not Applicable | ✓ Active License | ✗ Not Applicable |
| USDA Organic Certified Handling | ~ Select Lines | ✗ Not Applicable | ✓ Active | ✗ Not Applicable |
| ICH Q7 (API Manufacturing) | ✗ Not Applicable | ✓ Aligned | ✗ Not Applicable | ✓ Aligned |
| CDSCO Drug Manufacturing License | ✗ Not Applicable | ✓ Active | ~ Ayurvedic Drugs | ~ Where Applicable |
| APEDA Export Registration | ✓ Registered | ✓ Registered | ✓ Registered | ✓ Registered |
| Halal Certification | ✓ Available on Product | ✓ Available on Product | ✓ Available on Product | ~ Select Products |
| Third-Party Audit Openness | ✓ Welcome Anytime | ✓ Welcome Anytime | ✓ Welcome Anytime | ✓ Welcome Anytime |
The Documentation That
Gets Products Through Customs
Manufacturing is only half the job. The other half is getting your product from our facility into your destination market without customs delays, documentation queries, or regulatory hold-ups. Our export documentation team prepares market-specific compliance packages for every shipment — because the paperwork that clears the FDA-ORA differs from what German customs authorities require, and both differ from what Dubai Municipality needs.
From First Enquiry
to First Shipment
Whether you are sourcing a contract manufacturer for the first time or evaluating Jireh as a second-source supplier for an established brand, the engagement process is direct, transparent, and led by decision-making management — not junior account executives. Here is exactly how it works.
Facility Questions
Answered Directly
The questions international buyers and procurement teams most commonly ask before committing to a manufacturing partnership with an Indian CDMO — answered without marketing language.
Ready to See Our
Facilities and Build
Your Manufacturing Plan?
Request a virtual facility tour, schedule a third-party audit, or simply submit your product brief and let us propose the right manufacturing unit and approach for your brand. Ashish Daniel and the Jireh team respond to every serious enquiry within 24 hours — no gatekeeping, no intermediaries.
REQUEST FACILITY TOUR →Or contact us directly: shan@jnhub.com