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Best quality Heparin Manufacturer - Heparin Sodium (Porcine Source) – CSBIO Featured Image
  • Best quality Heparin Manufacturer - Heparin Sodium (Porcine Source) – CSBIO

Best quality Heparin Manufacturer - Heparin Sodium (Porcine Source) – CSBIO

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High quality Initial,and Buyer Supreme is our guideline to offer the ideal assistance to our shoppers.At present, we are striving our best to become amongst the ideal exporters inside our industry to satisfy shoppers more want for Heparin Adverse Effects, Heparin 25000, Heparin Injection Cost, Since the manufacturing facility founded, we have now committed on the progress of new products. While using the social and economic pace, we are going to continue to carry forward the spirit of "high high-quality, efficiency, innovation, integrity", and persist with the operating principle of "credit to start with, customer initially, top quality excellent". We'll make a amazing long run in hair output with our companions.
Best quality Heparin Manufacturer - 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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Best quality Heparin Manufacturer - Heparin Sodium (Porcine Source) – CSBIO detail pictures

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With a sound enterprise credit history, exceptional after-sales services and modern production facilities, we've earned an outstanding track record amongst our consumers across the whole world for Best quality Heparin Manufacturer - Heparin Sodium (Porcine Source) – CSBIO , The product will supply to all over the world, such as: Florence, Jeddah, United Arab Emirates, We have constructed strong and long co-operation relationship with an enormous quantity of companies within this business in Kenya and overseas. Immediate and specialist after-sale service supplied by our consultant group has happy our buyers. Detailed Info and parameters from the merchandise will probably be sent to you for any thorough acknowledge. Free samples may be delivered and company check out to our corporation. n Kenya for negotiation is constantly welcome. Hope to get inquiries type you and construct a long-term co-operation partnership.
    • Sales manager is very enthusiastic and professional, gave us a great concessions and product quality is very good,thank you very much!
    5 Stars By Deirdre from Indonesia - 2018.12.14 15:26
    The customer service staff is very patient and has a positive and progressive attitude to our interest, so that we can have a comprehensive understanding of the product and finally we reached an agreement, thanks!
    5 Stars By Jean Ascher from Jordan - 2017.02.14 13:19
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