Fully compliant with US FDA, EU Pharmacopoeia, and international clean-label standards. Sourced directly from Shaanxi herbal production reserves and processed in GMP certified workshops.
Headquartered in Xi'an, Shaanxi Province—the historical origin of Chinese Medicine trade and home to Qinling Mountains' bio-diversity—we blend ancestral botanicals with advanced chromatography isolation.
Equipped with 4 commercial continuous lines & 2 industrial pilot lines under rigorous GMP standards.
Collaborating with Xi'an Jiaotong, Northwest, and Xi'an University of Science and Technology.
In-house HPLC, Gas Chromatography, UV, and Heavy Metal testing with full lot COA documentation.
Seamless transition from laboratory test batches (1 kg) to metric ton container-scale contracts.
Supply Chain Security Note: Our facility is maintained with 18 senior technicians and 5 licensed TCM pharmacists. This deep botanical expertise eliminates cross-species contamination, verifying taxonomical accuracy via DNA fingerprinting and HPTLC marker authentication before entering the extraction reactors.
Global supply chain disruptions and stringent regulatory updates across North America and the EU are redefining how purchasing directors qualify extraction partners in Asia.
Traditional non-specific UV-Vis spectrometry allows deceptive adulteration with polyphenols or nitrogenous fillers. Sophisticated procurement teams now contractually mandate high-performance liquid chromatography (HPLC) or liquid chromatography-mass spectrometry (LC-MS) assays.
Consumers are actively rejecting maltodextrin, silicon dioxide, and synthetic carriers in end formulations. The market trend has pivoted towards 100% natural, spray-dried or freeze-dried matrix powders that preserve organoleptic fidelity without excipients.
Following strict EU alerts under RASFF regarding ethylene oxide residues in botanical raw materials, international importers require validated sterilization alternatives such as dry steam sterilization or controlled gamma irradiation.
The botanical extract industry has moved past rudimentary maceration. Modern botanical refining incorporates green chemistry, bio-fermentation, and microencapsulation to maximize bioavailability.
Eliminating toxic organic solvents (hexane, methanol) completely through supercritical CO₂ extraction preserves delicate terpenes and lipid-soluble components, making the extract fully acceptable for organic and COSMOS certified lines.
By inoculating plant extracts with beneficial microflora (such as our fermented Eurotium cristatum Golden Flower Tea and Cordyceps protocols), high-molecular glycosides are converted into high-permeability aglycones, tripling human metabolic bioavailability.
Hydrophobic substances such as Dihydroquercetin (DHQ) and Polyphenolic Antiviral agents struggle with oxidation and poor gastric stability. Nano-emulsion spray encasement ensures stability against gastric acidity and gradual enteric release.
Clear, direct answers regarding quality assurance protocols, global customs documentation, and logistics handling for procurement directors.
Every commercial batch undergoes botanical identity authentication overseen by our 5 licensed TCM pharmacists. We cross-verify via Thin Layer Chromatography (TLC), High-Performance Liquid Chromatography (HPLC) retention times, and DNA sequencing when sourcing species vulnerable to fraudulent adulteration (such as Epimedium or Cordyceps).
Every shipment is delivered with a lot-specific Certificate of Analysis (COA) containing exact assay percentages, moisture loss, total ash, particle mesh size, heavy metal limits (Lead, Arsenic, Cadmium, Mercury via ICP-MS), and microbiological status (Total Plate Count, Yeast/Mold, E. coli, Salmonella).
For standard stocked botanical powders and fruit powders, the MOQ starts at just 1 kg to facilitate R&D trial runs and analytical validation. For custom ratio extracts, specialized mesh sizes (e.g., 200 mesh), or custom carrier-free formulations, the pilot line MOQ typically begins at 25 kg to 100 kg.
Our extraction lines utilize strictly audited cultivation bases in Shaanxi and specialized resin filtration to intercept agricultural contaminants. All outgoing lots adhere to the strict threshold rules of USP <561> (Pesticides), European Pharmacopoeia (EP 2.8.13), and California Proposition 65 limits for heavy metals.
Standard packaging consists of food-grade, vacuum-sealed aluminum foil inner bags (1 kg or 5 kg) placed inside pharmaceutical-grade double polyethylene lined fiberboard drums (25 kg net weight). Dessicant inserts and nitrogen flushed atmospheres are implemented for moisture-sensitive extracts.
Yes. In addition to raw wholesale ingredients, our GMP facility operates high-speed sachet packing, cleanroom powder blending, instant functional mushroom coffee encapsulation, and blister-packaging lines. We provide private label support beginning at 500 units for finished branded formulations.