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Product profile
Customization
AvailableVarieties
Feed AdditiveComponent
Chemical Synthetic DrugsModel NO.
1046Type
The First ClassPharmacodynamic Influential Factors
Repeated MedicationStorage Method
Prevent High or LowTemperatureVeterinary Reg. No.
1024Transport Package
1kg/BagSpecification
1kg/bagTrademark
GRDROrigin
HebeiHS Code
30049090Production Capacity
500000Company profile
Business Type: Manufacturer/FactoryExport Year: 2011-05-11Nearest Port: XINGANG QINGDAOAverage Response Time: ≤15hTerms of Payment: LC, T/T, PayPal, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF
AI-Powered supplier vetting
SummaryHebei Guangren Pharmaceutical Technology Co., Ltd. is identified as a private Chinese manufacturer/factory specializing in more than 300 veterinary drug and animal-health products, including injections, powders, premixes, oral liquids, tablets, disinfectants, and feed additives. It reports five production lines, exports to multiple global regions, and holds BSCI, ISO 9000, and GMP certifications. The company describes structured raw-material, production-process, and multi-level product inspections, supported by 41–50 quality-control staff. Its stated R&D investment, sophisticated equipment, and product-development system indicate innovation activity, although the reported R&D engineering experience is below five years. Production lead time is within 15 working days off season and one month during peak season. Evidence is insufficient to confirm after-sales capability, customization capability, financial credibility, or specific customer cases.
Supplier typeThe supplier is explicitly classified as a Manufacturer/Factory and is a private company based in Shijiazhuang, Hebei, China. Its stated business focuses on manufacturing more than 300 veterinary drug and animal-health products, although one slice also describes the associated company nature as a trading company.
CertificationsThe supplier reports holding BSCI, ISO 9000, and GMP management-system certifications. These certifications provide explicit evidence of formal compliance and quality-management credentials, though the slices do not specify certificate scope, issuing bodies, or validity dates.
R&D capabilityThe company states that it invests in sophisticated equipment and new-product development, operates a scientific R&D system, and introduces dozens of new products annually. These statements explicitly support ongoing product-development activity and product-structure optimization, although the reported total R&D engineer experience is below five years.
Production capacityThe supplier reports five production lines, production of 500,000,000 veterinary-medicine boxes, more than 300 product types, 41–50 quality-control staff, and multi-level inspections. It states an off-season fulfillment time within 15 working days and a peak-season lead time of one month, providing explicit evidence of established production and quality-control capacity.
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