Standardized
cGMP-Compliant Standardized Botanical Powder Extracts
At IES Biotech Co., Ltd., our standardized botanical powder extracts are produced under strict quality control standards. Each batch is engineered to deliver guaranteed active compound assays, reproducible phytochemical profiles, and optimal physical properties for seamless manufacturing integration.
Utilizing advanced extraction technologies—including aqueous extraction, solvent fractionation, spray drying, and vacuum crystallization—we serve international procurement teams with ingredients that exceed rigorous global safety and regulatory requirements.
- HPLC / UV / GC Quantified Active Markers
- 20+ Years Phytochemical Manufacturing Expertise
- Batch-Specific Certificate of Analysis (COA)
- USP / EP / CP Pharmacopeia Compliance
- Pesticide Residue & Heavy Metal Tested
- Non-GMO, Allergen-Free & Irradiation Certified
Standardized Powder Extracts Catalog
Standardized
Standardized
Cape Jasmine Extract
High Assay
Centella asiatica Extract
Standardized
Chrysanthemum indicum Extract
Standardized
Cornus officinalis Extract
High Assay
Cyanotis arachnoidea Extract
Standardized
Engelhardia roxburghiana Extract
Standardized
Garlic Extract
Standardized
Isatis indigotica (Banlangen) Extract
High Assay
Paeonia lactiflora (White Peony) Root Extract
Standardized
Polygonum multiflorum (Fo-Ti) Root Extract
Standardized
Salvia rosmarinus (Rosemary) Extract
High Assay
Vine Tea Extract
Technical Specifications & Quality Parameters
IES Biotech Co., Ltd. provides full analytical verification and batch documentation with every commercial order.
| Analytical Parameter | Specification Target | Testing Methodology | B2B Quality Assurance |
|---|---|---|---|
| Active Marker Content | Guaranteed Target Range (1% - 98%) | HPLC / UV-Vis / GC / Titration | Fully analytical Certificate of Analysis (COA) per batch |
| Heavy Metal Limits | Pb < 2.0 ppm, As < 1.0 ppm, Cd < 1.0 ppm, Hg < 0.1 ppm | ICP-MS / AAS | Complies with USP <232><233> and EP limits |
| Pesticide Residue | Below EU & USP Maximum Residue Limits | GC-MS/MS / LC-MS/MS (500+ Screen) | Complete multi-residue screening report |
| Microbiological Quality | Total Plate Count < 1,000 cfu/g, Yeast & Mold < 100 cfu/g | USP <2021><2022> / EP standards | Pathogen-free (Salmonella, E. coli, S. aureus Negative) |
| Physical Parameters | Loss on Drying < 5.0%, Mesh Size 80 - 100 mesh | Gravimetric / Sieve Analysis | Optimized bulk density and powder flowability |
OEM / Contract Manufacturing Services
We partner with global formulators to engineer customized particle sizes, extraction ratios, and target phytochemical concentrations.
Custom Standardization
Tailored marker-compound ratios and custom purity targets tailored to your formulation's exact clinical or chemical requirements.
Particle Granulation
Granulation, microencapsulation, and particle size customization (80-200 mesh) to ensure dust-free direct compression or capsule filling.
Regulatory & Technical Support
Complete regulatory dossiers, TDS, MSDS, Allergen statements, Non-GMO certificates, and stability testing support for global registration.
Request Bulk Pricing & Sample Kits
Contact the technical sales team at IES Biotech Co., Ltd. for product specifications, batch COAs, custom quote options, or free sample evaluation.
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