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Factory wholesale Heparin 25000 - Heparin Sodium (Porcine Source) – CSBIO Featured Image
  • Factory wholesale Heparin 25000 - Heparin Sodium (Porcine Source) – CSBIO

Factory wholesale Heparin 25000 - Heparin Sodium (Porcine Source) – CSBIO

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High quality Very first,and Consumer Supreme is our guideline to offer the most beneficial service to our consumers.At present, we're attempting our greatest to be among the top exporters in our area to fulfill buyers far more need to have for Dalteparin And Warfarin, Heparin 40 Mg, Fragmin Price, We acquire high-quality as the foundation of our results. Thus, we focus over the manufacture on the finest top quality goods. A strict quality management system has been created to guarantee the caliber of the merchandise.
Factory wholesale Heparin 25000 - Heparin Sodium (Porcine Source) – CSBIO Detail:

INDICATIONS:
Prevention and treatment of thrombosis or thrombotic diseases (such as myocardial infarction, thrombophlebitis, pulmonary embolism and so on); also used in the treatments of disseminated intravascular coagulation (DIC) derived from all kinds of reasons; hemodialysis, extra-corporeal circulation, catheterization, microvascular surgery and anticoagulation treatment of some blood samples and instruments.

COMPANY ADVANTAGE
1.full product Chains:
We have the full product Chains, which starts from the Porcine mucosa with be processed to Crude heparin, Heparin sodium API that could be depolymerized to the API of Enoxaparin sodium, Dalteaprin sodum and Nadroparin calcium. We could control the product from the starting material and make sure the tracebility which is required by the regulated market. At present, we have our own crude heparin workshop, which could help us to not only control the cost bust also assure the quality of our product.
2.APIs’ Production Lines：
Facilities and Equipment Systems
There are dedicated production workshops respectively for Heparin API, Enoxaparin Sodium API and Dalteparin Sodium&Nadroparin Calcium API. These three workshops are all established and have their respective dedicated production equipments, HVAC system and purify water system, which could avoid the cross contamination.
3.Product qualification
For Heparin Sodium API, we have passed the followings audits, US-FDA, EDQM, CFDA, Germany/Korean and Turkey authority, CEP, EIR-LETTER, China and Germany GMP are available.
4.Production capacity is enough：Heparin Sodium API: 5 million mega
5.We basically estsabilshed GMP Six-system that can comply with the standard of EU GMP，US FDA CGMP and Chinese GMP which could make sure our product comply with the international quality systems.
6.The company is located in the Zhengding area of China (Hebei) Pilot Free Trade Zone, close to Shijiazhuang Airport and the high-speed railway station, with a good transportation location. On August 26, 2019, the State Council issued the “Overall Plan for China (Hebei) Pilot Free Trade Zone”. The Zhengding area focuses on the development of bio-medicine, international logistics and other industries. We will strive to build the company into a leading enterprise in the domestic heparin industry.
7.Main market: Italy, Russia, Ukraine, Belarus, Indian, Korean, Argentina, Turkey, Iran and so on.
8.Payment: TT in advance
Delivery details: within in 30days after confirmed the order by air
Flow Chart of Heparin Sodium
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Products Specification (EP)

TESTS

SPECIFICATIONS

Characters

White or almost white, hygroscopic powder.

Solubility

Freely soluble in water

Identification

A. It complies with the requirements described under Assay

B. The ratio of anti-factor Xa activity to anti-factor IIa activity ranges between 0.9~1.1.

C. 1H-NMR Spectrum: comply with the Ph. Eur. specification of heparin about 1H-NMR requirements.

D. The principal peak in the chromatogram obtained with test solution is similar in retention time and shape to the principal peak in the chromatogram obtained with reference solution.

E. It complies with the test for sodium.

Appearance of solution

The solution is clear and not more intensely coloured than intensity 5 of the range of reference solutions of the most appropriate color.

pH

5.5 ~ 8.0

Nucleotide impurities

Absorbance at 260 nm: ≤0.15

Protein

≤0.5%

Related substances

A. Sum of dermatan sulfate and chondroitin sulfate: not more than the area of the peak due to dermatan sulfate and chondroitin sulfate in the chromatogram obtained with reference solution (e) (2.0 per cent);

B. Any other impurity: no peak with an area greater than 0.01 times the area of the peak due to dermatan sulfate and chondroitin sulfate in the chromatogram obtained with reference solution (e) is detected (corresponding to a disregard limit of 0.02 per cent)

Nitrogen

1.5%~2.5%

Sodium content

10.5%~13.5%

Loss on drying

≤8.0%

Bacterial endotoxin

Less than 0.01 IU/IU of heparin

Potency

≥180 IU/mg

Products Specification (USP)

TESTS

SPECIFICATIONS

Characters

White or almost white, hygroscopic powder.

Solubility

Freely soluble in water

Identification
  1. 1H-NMR Spectrum: No unidentified signals greater than 4% of the mean of the height of signals 1 and 2 are present in the following ranges: 0.10–2.00, 2.10–3.20, and 5.70–8.00 ppm. No signals greater than 200% of the mean of the height of signals 1 and 2 are present in the 3.75–4.55 ppm for porcine heparin .
  2. Chromatographic: The retention time pf the major peak of the Sample solution corresponds to that of the Standard solution.
  3. Anti-factor Xa to anti-factor Ⅱa ratio: 0.9 – 1.1
  4. Molecular weight: M is NMT 20%, M is between 15,000 Da and 19,000 Da, and the ratio of M to M is NLT 1.0.
  5. A solution of Heparin Sodium imparts an intense yellow color to a nonluminous flame.

Appearance of solution

The solution is clear and not more intensely coloured than intensity 5 of the range of reference solutions of the most appropriate color.

pH

5.0 ~ 7.5

Nucleotide impurities

NMT 0.1% (w/w) is found.

Protein

NMT 0.1% (w/w) is found.

Related substances
  1. Proceed as directed in Identification A. No features associated with oversulfated chondroitin sulfate are found between 2.12 and 3.00 ppm.

 

  1. Proceed as directed in Identification B. No peaks corresponding to oversulfated chondroitin sulfate should be detected eluting after the heparin peak.

Loss on drying

≤5.0%

Bacterial endotoxin

It contains NMT 0.03 USP Endotoxin Units/USP Heparin Unit.

Potency

≥180 IU/mg

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Factory wholesale Heparin 25000 - Heparin Sodium (Porcine Source) – CSBIO detail pictures

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Our corporation puts emphasis about the administration, the introduction of talented staff, plus the construction of team building, attempting hard to improve the quality and liability consciousness of team members. Our organization successfully attained IS9001 Certification and European CE Certification of Factory wholesale Heparin 25000 - Heparin Sodium (Porcine Source) – CSBIO , The product will supply to all over the world, such as: Rwanda, Australia, Bhutan, In the future, we promise to keep offer the high quality and more cost-effective products, the more efficient after sales service to our all customers all over the world for the common development and the higher benefit.
    • This enterprise in the industry is strong and competitive, advancing with the times and develop sustainable, we are very pleased to have a opportunity to cooperate!
    5 Stars By Joyce from Czech - 2017.06.16 18:23
    The factory can meet continuously developing economic and market needs, so that their products are widely recognized and trusted, and that's why we chose this company.
    5 Stars By Adam from Argentina - 2017.10.27 12:12
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