Advanced Spray-Drying
Engineered fat powders and microencapsulated lipids offering enhanced water solubility, superior oxidative stability, and prolonged shelf life for sports & clinical nutrition powders.
Zeon Lifesciences Ltd offers comprehensive Contract Research and Manufacturing Services (CRAMS) tailored for global dietary supplement brands, pharmaceutical firms, and D2C wellness companies. Backed by over 38 years of technical mastery, our DSIR-recognized R&D center serves as an innovation engine, developing science-backed, high-potency formulations engineered for shelf stability, bioavailability, and global regulatory acceptance.
Our integrated manufacturing campus in Himachal Pradesh, India, combines pharmaceutical-grade cleanroom environments, automated dosage lines, and advanced analytical testing suites. From raw material characterization to pilot trials and full-scale commercial manufacturing, our turnkey approach minimizes time-to-market while reducing operational risks for international importers.
Our research campus handles complex formulation requirements, excipient compatibility testing, and pilot scale runs before initiating commercial production. This ensures consistent batch reproducibility and zero rework during commercial scale-up.
We provide full-spectrum scientific services designed to convert novel nutraceutical concepts into commercially viable, consumer-preferred health products.
Development of bespoke formulations across tablets, capsules, nutritional powders, diskettes, and oral liquids tailored to target demographic requirements and precise nutritional claims.
Rigorous vendor qualification, active ingredient assaying, marker-compound verification, and botanical extract standardization to ensure consistent biological efficacy.
Utilization of solid dispersion matrices, spray-dried liposomal technology, and nanoencapsulation to maximize targeted nutrient absorption and GI tolerance.
Accelerated and real-time stability protocols executed inside ICH-compliant chambers to establish validated expiration dating, packaging compatibility, and overage requirements.
Advanced taste-masking technologies, natural flavor system integration, and texture enhancement for oral liquids, chewables, and functional powder drink mixes.
Comprehensive technical data packages, COAs, stability summaries, allergen declarations, and non-GMO compliance papers formatted for frictionless international customs clearance.
Our research team actively pushes the frontiers of food tech and phyto-pharmaceutical formulation to deliver market-differentiating product lines.
Engineered fat powders and microencapsulated lipids offering enhanced water solubility, superior oxidative stability, and prolonged shelf life for sports & clinical nutrition powders.
Solid dispersion techniques paired with pharmacokinetic (PK/PD) studies to dramatically boost systemic bioavailability and therapeutic efficiency of natural antioxidants.
Cost-effective, highly soluble cocoa alternative powders and instant frappe matrices delivering rich organoleptic properties without compromising dietary fiber or nutritional profiles.
Institutional partnerships to design and execute human clinical trials, enabling brand owners to back premium structural/functional health claims with peer-reviewed evidence.
Key technical and operational questions answered by our R&D leadership team.
We offer contract formulation and manufacturing across five core dosage platforms: compressed tablets & caplets, hard gelatin & HPMC encapsulation, functional & nutritional powders, oral liquids & syrups, and specialized nutritional diskettes. Each platform is supported by custom release rate engineering and stability optimization.
Yes. Our technical team works directly with accredited contract research organizations (CROs) and university research hospitals to design human clinical trial protocols, conduct bio-equivalence studies, validate structural/functional claims, and author scientific papers for publication.
All newly developed formulations undergo rigorous stability testing protocols inside ICH-compliant environmental chambers (Zone IVB conditions for tropical exports). Testing includes HPLC assaying of active nutrients, dissolution profiling, microbial challenge testing, and packaging integrity assays.
Absolutely. We maintain a global network of vetted active pharmaceutical ingredient (API) and nutraceutical raw material vendors. Our quality control laboratory performs identity testing, heavy metal screening, pesticide residual testing, and allergen assays on all incoming raw material lots.
We utilize specialized solid dispersion processing, fluid-bed microencapsulation, spray-drying, and liposomal delivery systems to improve the dissolution rates and intestinal absorption of poorly soluble botanical actives and hydrophobic vitamins.
Yes. Every new CRAMS project transitions through representative pilot scale runs in dedicated pilot bays. This stage allows our process engineers to optimize granulation parameters, compression speeds, and filling tolerances to guarantee seamless scaling during commercial production runs.
Partner with an audit-ready, DSIR-recognized CRAMS provider to streamline formulation development, clinical testing, and global export packaging.