Explore our core CRO/CDMO solutions designed to benchmark, screen, and validate botanical active ingredients across diverse origins and global regulatory frameworks.
In botanical pharmacology and high-tier nutraceutical OEM/ODM, the concept of origin transcends simple national borders. It is governed by microclimates, pedology, agronomic stress factors, and botanical epigenetics.
A single herb harvested in disparate provinces yields wildly divergent secondary metabolites. Known historically as 'Daodi' material in Traditional Chinese Medicine, our scientific mapping determines the precise altitude, ultraviolet exposure, and mineral profile that triggers peak expression of active polyphenols, saponins, and alkaloids.
Harvesting four weeks off-cycle can collapse active content by up to 60%. Our ODM place-of-origin analytical services quantify metabolic shifts throughout vernal and autumnal cycles, arming procurement teams with empirical harvest-window parameters rather than speculative trading timelines.
True 'Best Origin' is as much about purity as it is about potency. Our analytical laboratories benchmark regional soil geologies for heavy metals (lead, cadmium, arsenic, mercury) and persistent organic pollutants, ensuring target crops inherently satisfy USP, EP, and FDA botanical monographs.
Combining multi-generational botanical provenance with cutting-edge automated extraction, intelligent process control, and end-to-end analytical traceability.
Eliminating thermal degradation through automated, closed-loop continuous countercurrent extraction lines. Programmable PLC interfaces govern solvent polarity, temperature curves, and residence time with sub-second responsiveness, reducing thermal decay of delicate phytochemical markers.
Precision fraction separation using pilot-scale ceramic membrane modules and high-selectivity macroporous adsorption resins. This enables targeted compound enrichment (reaching up to 98% pure fraction concentrates) while stripping pigments, residual solvent complexes, and ash content.
Every commercial CDMO batch undergoes in-line NIR and chromatographic fingerprint monitoring. Data feeds directly into our centralized LIMS and ERP suites, guaranteeing identical bioavailability and organoleptic properties whether executing a 50kg pilot assay or a 100-metric-ton production run.
International nutraceutical brands, pharmaceutical formulators, and cosmeceutical developers face escalating regulatory thresholds. Contract development must bridge empirical agricultural output with rigid documentation.
Raw UV-Vis testing is no longer acceptable to premium Western regulators. Our laboratory deploys validated HPLC, HPTLC, and GC-MS chromatographic fingerprinting capable of identifying adulterants, synthetic spikes, and verifying true place-of-origin ratios down to parts-per-billion.
We provide turnkey regulatory documentation for global applications—spanning FDA NDI (New Dietary Ingredient), GRAS dossiers, European EFSA Novel Food files, and cGMP-compliant Batch Production Records (BPR), ensuring zero import friction.
Operating under an entrusted contract model, formulas, custom extraction solvents, and clinical trial matrices remain 100% proprietary to the commissioning brand. Comprehensive non-disclosure agreements guard your competitive edge at every scale.
Whether engaging for standalone analytical method development or a multi-year drug development pipeline, our transparent milestones de-risk your investment.
Phytochemical benchmarking across soil profiles, micro-climates, and harvest windows to pinpoint peak bio-active compound density.
Establishing high-precision analytical assays using HPLC, HPTLC, GC, and chromatographic fingerprinting for absolute batch reproducibility.
Pilot-line extraction, dynamic chromatography separation, membrane purification, and vacuum low-temperature spray drying parameters.
Validating bioactivity through cellular in vitro models, LD50 acute toxicity, subchronic toxicology, and mutagenic genotoxicity panels.
Executing human pilot clinical trials for dietary efficacy substantiation or Phase I–IV human studies intended for drug registrations.
Full commercial processing across raw active powders, concentrated oils, or finished dosage forms (capsules, softgels, oral liquids, tablets).
Transforming origin-verified raw phytochemical extracts into high-potency, commercially viable delivery formats across core global industries.
Engineered for brand owners requiring stable active concentrations, organoleptic perfection, and instant water solubility. Applications include standardized powders for sachet drinks, effervescent formulations, enteric-coated capsules, and fast-release softgel matrices.
Supporting pharmaceutical innovators advancing botanical drugs through multi-target action. We synthesize clinical lots under cleanroom environments, standardizing complex multi-herb formulas into ultra-precise oral liquids, injectable grades, and enteric solid tablets.
Developing safe, skin-penetrating plant bio-actives for anti-aging, barrier repair, and pigmentation reduction. Formats encompass sub-micron emulsions, cold-pressed therapeutic oils, liposomal suspensions, and water-dispersible botanical pastes.
Over 14 years of research partnership with industry-defining state enterprises, listed pharmaceutical conglomerates, and university research clinics.
Beijing Tongrentang Group
CR Sanjiu Pharmaceutical
Sunflower Pharmaceutical
Livzon Pharmaceutical
Dihon Pharmaceutical
Golden Throat Group
Yangtzi River Pharma
Beihai Gofar Biological
Humanwell Healthcare
SCIMYTH Pharmaceutical
Hanfang Pharmaceutical
Luoxin Pharmaceutical
Zhongsheng Pharmaceutical
Brilliance & Abundance
Apeloa Pharmaceutical
Heng Chang Pharma
Baotou TCM
Kamp Medicine
Santo Pharmaceutical
Kangshou Pharmaceutical
Juwang Pharmaceutical
Tcmages Pharmaceutical
Ruihe Pharmaceutical
CR Jinchan Pharma
Kangmei Pharmaceutical
Tianjicaotang Pharma
Kingstone Unite Pharma
Shuguang Hospital TCM
Hunan Affiliated TCM Hosp.
First Hosp. Hunan TCM
Direct answers to core queries regarding analytical validation, audit readiness, geo-origin authentication, and batch scaling.
Immediate procurement and project initiation for origin-verified testing, screening, clinical studies, and OEM extract production.
