Product Certification&
Enterprise Certification
Country: China (Mainland)
Business Type:Trading Company
Tel: 86-27-84492310
Tel: 008618986076206
Tel: +86 27 84492310
Tel: WhatsApp +8615927784577
Tel: +8618071739296
Mobile: +8615207100586
Tel: 86-27-84492310
Fax: 86-27-84402310
URL: http://www.vanzpharm.com/en/index.html
Province/state: Hubei
City: JIAYU
Street: FANHU INDUSTRY PARK
MaxCard:
CAS NO.967-80-6
98%(1-1000000)Gram
967-80-6
Hubei Vanz Pharm Co. Ltd. is the leading manufacture of APIs, supplements raw powder and some customization products. located in Hubei province, China.
We are one of the most professional company in pharm/chemical industry for more than 10 years.
We export to many countries and area with very competitive price, high quality, good service. Excellent capacity to support your business. Fast delivery.
Contact me. Start good cooperation.
Superiority
1.Professional synthesis laboratory and manufacture /production base.
2.Strong synthesis team and service team. Professional data management.
3.We provide the professional test data and product information ,eg: MSDS,COA,MOA,TDS,DMF
4..Any inquiries will be replied within 48 hours.
5.All kinds of shipping methods, eg: FedEx,DHL,TNT,BY SEA and BY AIR.
6.Shipping information includes Commercial Invoice,Packing List,COA,BSE/TSE.If your markets have any special requirements, please let us know.
7.We can accept various payment methods,L/C,T/T, etc.
8.Professional packaging can be according the customers’ requirement.
9.Product application: Medicinal Chemistry 、 Biomedicine、 Pharmaceutical intermediate、 Chemistry experiment 、Biological experiments 、Chemical reagent , for R&D use only.
The reason why choose us :)
Our Guarantee on quality
1)Purchasing
Thorough market research, understand the price of raw materials and performance.To the procurement source to understand fully, and fully guarantee the quality of the procurement of raw materials.
2) Inspection
Four steps: sampling, sample pretreatment, measuring and data processing.
3) Producing
a)Each operator must do self-inspection of producs and make the corresponding inspection records.
b)Full-time inspectors through check the operator self-inspection, and review and sign in the corresponding record. Full-time inspection is responsible for inspection of finished product, and make the finished product incoming inspection records.
4) Before selling
Test result can be provided before selling.
Third-party detection institution is allowed if you are not satisfied with test results.
Sulfaquinoxaline sodium salt shows the presence of all antimicrobial residues at concentration higher than the drugs' maximum residue limit (MRL) of 100 μg/kg until two days after discontinuation of the medication.
Superiority
1.Professional synthesis laboratory and manufacture /production base.
2.Strong synthesis team and service team. Professional data management.
3.We provide the professional test data and product information ,eg: MSDS,COA,MOA,TDS,DMF
4..Any inquiries will be replied within 48 hours.
5.All kinds of shipping methods, eg: FedEx,DHL,TNT,BY SEA and BY AIR.
6.Shipping information includes Commercial Invoice,Packing List,COA,BSE/TSE.If your markets have any special requirements, please let us know.
7.We can accept various payment methods,L/C,T/T, etc.
8.Professional packaging can be according the customers’ requirement.
9.Product application: Medicinal Chemistry 、 Biomedicine、 Pharmaceutical intermediate、 Chemistry experiment 、Biological experiments 、Chemical reagent , for R&D use only.
The reason why choose us :)
Our Guarantee on quality
1)Purchasing
Thorough market research, understand the price of raw materials and performance.To the procurement source to understand fully, and fully guarantee the quality of the procurement of raw materials.
2) Inspection
Four steps: sampling, sample pretreatment, measuring and data processing.
3) Producing
a)Each operator must do self-inspection of producs and make the corresponding inspection records.
b)Full-time inspectors through check the operator self-inspection, and review and sign in the corresponding record. Full-time inspection is responsible for inspection of finished product, and make the finished product incoming inspection records.
4) Before selling
Test result can be provided before selling.
Third-party detection institution is allowed if you are not satisfied with test results.