Precision-manufactured raw ingredients and customized formulations engineered for nutraceutical, cosmetic, functional beverage, and dietary supplement formulations.
Operating directly out of the Qinling Mountain botanical corridor in Xi'an, Torzi Biotech integrates primary raw botanical sourcing, advanced chromatographic fractioning, and complete OEM dosage manufacturing under a unified cGMP-compliant quality architecture.
Full 12,447 m² infrastructure verified independently by SGS Group. From cleanrooms to pressurized storage tanks, every processing zone meets stringent international sanitary criteria.
In-house quality inspection laboratory outfitted with dual HPLC systems, GC solvent residue testers, and Atomic Absorption Spectrometers for accurate quantification of active markers and heavy metals.
Agile commercial engineering supporting low-MOQ pilot validation from 1 kg up to multi-ton continuous manufacturing contracts without compromising standard deviation across lot runs.
Custom dosage development including vegetable capsules, micro-tablets, stick sachets, and specialized pre-blends backed by full regulatory packaging, labeling, and export dossier assistance.
The botanical extract sector is undergoing a profound paradigm shift driven by advancements in analytical chemistry, bioavailability technologies, and consumer skepticism surrounding synthetic excipients. Today's commercial formulators require substantiated biochemical potency rather than generic raw powders:
Procurement teams across North America, Europe, and the Asia-Pacific region are overhauling vendor qualification criteria to insulate their brands from regulatory recalls, adulteration liabilities, and supply disruptions:
Clear, direct answers to common questions raised by procurement directors, quality assurance managers, and product formulators.
Every raw botanical incoming lot is subjected to macroscopic, microscopic, and High-Performance Thin-Layer Chromatography (HPTLC) fingerprint analysis against authoritative pharmacopeial reference standards. For high-risk species, DNA barcoding is deployed to ensure 100% genuine botanical origin before extraction begins.
Each batch is shipped with a comprehensive Certificate of Analysis (COA) specifying active assay percentages, residual solvent quantities (GC), microbiological profiles (total plate count, yeast/mold, E. coli, Salmonella), and heavy metals tested via AAS or ICP-MS. Safety Data Sheets (SDS), Kosher/Halal, and Organic certificates are available on demand.
For standard bulk powders and botanical extracts, our baseline MOQs start as low as 1 kg to 25 kg to facilitate pilot bench runs and laboratory validations. For customized OEM private label capsule packaging, bottle packing, or custom sachet blending, production MOQs start at 500 finished consumer units.
Standard bulk export orders utilize food-grade multi-layer pharmaceutical polyethylene liner bags sealed inside high-density fiberboard drums (25 kg net weight). Moisture-sensitive active monomers and freeze-dried superfood powders are flushed with food-grade nitrogen and heat-sealed in thick foil-laminated barrier pouches with desiccants.
Yes. Our milling, pulverizing, and screening stages can customize mesh sizing between 80 mesh and 300 ultra-fine mesh depending on whether your final formulation is destined for high-speed automated capsule filling, tablet direct compression, liquid beverage suspension, or topical emulsion creams.
Yes. All finished extracts comply strictly with European Pharmacopoeia (EP), United States Pharmacopeia (USP), and California Proposition 65 limits for lead, arsenic, cadmium, and mercury. Pesticide screenings cover over 400 compounds via LC-MS/MS and GC-MS/MS to ensure compliance across strictly regulated markets.
Connect directly with our chemical engineers and commercial procurement specialists. Obtain full technical specifications, batch Certificates of Analysis, and complimentary evaluation samples dispatched within 24 hours.