Verified bulk raw materials, functional additives, and clean-label formulations ready for global OEM/ODM deployment.
Empowering global wellness brands through rigorous analytical testing, custom formulation science, and multi-jurisdictional cGMP compliance.
Operating from dedicated pharmaceutical-grade manufacturing blocks in Paonta Sahib, Himachal Pradesh, and corporate hubs in Noida, India, our facilities leverage US FDA registration, FSSC 22000 (Intertek certified), GMP, HACCP, FSSAI, AYUSH, and Halal accreditations. With 38+ years of expertise, we manage high-capacity lines capable of yielding 400 million tablets, 140 million hard/soft gel capsules, 70 million oral liquid bottles, 100 million nutritional diskettes, and 35,000 MT of functional powders annually.
Information gain in modern procurement rests on analytical verification. Our fully instrumented quality control testing facilities house High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis Spectrophotometry, Heavy Metal Inductively Coupled Plasma Mass Spectrometry (ICP-MS), and automated dissolution apparatuses. Every batch undergoes physical, chemical, micro-biological, and stability verification under ICH climate zone conditions (Zone IVb) to ensure label claim integrity over shelf life.
Standardized dosage matrices engineered to handle complex bioavailability challenges and custom active ingredient release profiles.
| Dosage Format | Annual Production Capacity | Technical Features & Delivery Technologies | Regulatory Compliance Standards |
|---|---|---|---|
| Tablets & Caplets | 400 Million Units | Bi-layer compression, enteric coating, sustained-release (SR), chewable, effervescent tablets. | US FDA, FSSC 22000, GMP, AYUSH |
| Hard & Soft Gel Capsules | 140 Million Units | Vegetable HPMC & Gelatin shells, liquid-filled hard capsules, low-humidity probiotic encapsulation. | Halal Certified, FSSC 22000, cGMP |
| Nutritional & Functional Powders | 35,000 Metric Tons | Fluidized-bed agglomeration, instantized whey/plant proteins, micro-encapsulated active blends. | HACCP, ISO 22000, FSSAI Export Pack |
| Oral Liquids & Syrups | 70 Million Bottles | Aseptic liquid filling, taste-masked pediatric/geriatric syrups, herbal decoctions, single-serve shots. | US FDA Registered, WHO-GMP |
| Nutritional Diskettes & Chewables | 100 Million Units | High-protein biscuits/diskettes, fortified functional snacks, controlled micronutrient dispersion. | FSSAI, ISO 9001:2015, Halal |
Strategic analysis of global supply chain shifts, regulatory evolution, and consumer demand drivers shaping B2B contract manufacturing.
Global buyers no longer accept simple paper certificates. Modern procurement mandates third-party batch verification, heavy metal screening (Pb, Cd, Hg, As), pesticide residue testing via LC-MS/MS, and DNA barcode identification for botanical extracts to prevent adulteration.
Standard powders are rapidly losing market share to liposomal delivery systems, cyclodextrin complexation (such as Alpha-Cyclodextrin fat encapsulation), and micro-encapsulated active botanicals that protect sensitive active compounds against gastric degradation.
Excipient reform is sweeping global markets. Formulation requests increasingly specify synthetic additive replacement—utilizing natural maltodextrin carriers, yeast extract umami enhancers, and organic beetroot colorants instead of titanium dioxide and artificial dyes.
How our technical teams escort your supplement formulation from concept screening to export-ready container dispatch.
Scientific review of active ingredients, target dosage compatibility, excipient selection, and destination country regulatory limits.
Analytical testing of incoming active raw materials and excipients via HPLC, GC, FTIR, and microbiological identification assays.
Trial execution on production-representative equipment to optimize compression pressure, blend uniformity, and taste masking.
Automated high-speed granulators, tablet presses, encapsulation machines, and liquid filling lines operating in class 100,000 cleanrooms.
Assay validation, dissolution testing, heavy metal clearance, allergen verification, and accelerated ICH stability chamber retention.
Compilation of Certificate of Analysis (CoA), Free Sale Certificates, Halal documentation, CTD regulatory dossiers, and export logistics.
Technical and operational answers to common queries submitted by procurement heads, R&D directors, and brand owners.
OEM (Original Equipment Manufacturing): We manufacture products strictly according to your customized formulation specifications, active ingredient inputs, and precise master batch records.
ODM (Original Design Manufacturing): We provide ready-to-market, clinically evaluated base formulations from our catalog of over 850 commercialized SKUs. We customize flavor profiles, dosage forms, and brand packaging, dramatically reducing your time to market.
Our in-house analytical laboratories implement High-Performance Liquid Chromatography (HPLC) for active marker quantification, Gas Chromatography (GC) for residual solvent and fatty acid profiling, Atomic Absorption Spectrophotometry (AAS) / ICP-MS for heavy metals, and validated micro-biological assays for total plate count, yeast/mold, E. coli, and Salmonella screenings.
Our manufacturing ecosystem operates under US FDA Registration, FSSC 22000 (certified by Intertek), WHO-GMP, HACCP, ISO 9001:2015, ISO 22000, Halal Certification, and AYUSH (Ayurvedic ministry) licensing. We regularly provide Common Technical Document (CTD) dossiers, stability studies, and Free Sale Certificates required by international regulatory authorities.
Probiotic and enzyme formulations are handled in specialized low-humidity environmental suites (RH < 20%). We employ live strain CFU overage strategies, micro-encapsulation, cold-chain ingredient storage, and moisture-barrier packaging (Alu-Alu blisters, HDPE bottles with active desiccant caps) to guarantee label claims throughout shelf life.
R&D formulation screening and prototype sampling typically require 2 to 3 weeks. Upon formula freeze, artwork sign-off, and raw material qualification, commercial cGMP batch production and testing packaging are completed within 4 to 6 weeks.
Building sustainable, high-margin, and audit-ready supply chains for global healthcare, pharmaceutical, and D2C brand leaders.
Our team brings together pharmaceutical scientists, food technologists, Ayurvedic doctors, and regulatory affairs specialists. We ensure every ingredient selection balances efficacy, organoleptic appeal, cost-efficiency, and destination country compliance.
Every production batch receives an immutable electronic Master Production Record (eMPR). Raw materials are sourced exclusively from pre-audited, qualified suppliers, enabling complete lot-to-carton traceability.
Exporting across 60+ countries, our international logistics desk manages container consolidation, climate-controlled shipping options, customs documentation, and country-specific barcode/labeling requirements.
Partner with a US FDA-registered, FSSC 22000-certified OEM/ODM contract manufacturer and testing factory. Get customized formulation support, analytical testing documentation, and rapid market deployment.