Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech Co., Ltd. Shu-Lin TW
02 1APOTEX PHARMACHEM INC. Brantford CA
03 1BIOCON LIMITED Bangalore IN
04 1BIOCON LIMITED Bengaluru IN
05 1CONCORD BIOTECH LIMITED Ahmedabad IN
06 1DAIICHI SANKYO CO., LTD. Tokyo JP
07 1KYOWA HAKKO BIO CO., LTD. Tokyo JP
08 1LEK PHARMACEUTICALS D.D. Ljubljana SI
09 1LIVZON NEW NORTH RIVER PHARMACEUTICAL CO., LTD. Qingyuan City CN
10 1Ranbaxy Laboratories Limited Gurgaon IN
11 1TAPI NL B.V. Amsterdam NL
12 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Certificate Number : R1-CEP 2004-168 - Rev 01
Status : Valid
Issue Date : 2021-03-04
Type : Chemical and TSE
Substance Number : 2059
77
PharmaCompass offers a list of Pravastatin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pravastatin manufacturer or Pravastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pravastatin manufacturer or Pravastatin supplier.
PharmaCompass also assists you with knowing the Pravastatin API Price utilized in the formulation of products. Pravastatin API Price is not always fixed or binding as the Pravastatin Price is obtained through a variety of data sources. The Pravastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vasten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vasten, including repackagers and relabelers. The FDA regulates Vasten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vasten API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Vasten manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vasten supplier is an individual or a company that provides Vasten active pharmaceutical ingredient (API) or Vasten finished formulations upon request. The Vasten suppliers may include Vasten API manufacturers, exporters, distributors and traders.
click here to find a list of Vasten suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vasten CEP of the European Pharmacopoeia monograph is often referred to as a Vasten Certificate of Suitability (COS). The purpose of a Vasten CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vasten EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vasten to their clients by showing that a Vasten CEP has been issued for it. The manufacturer submits a Vasten CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vasten CEP holder for the record. Additionally, the data presented in the Vasten CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vasten DMF.
A Vasten CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vasten CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Vasten suppliers with CEP (COS) on PharmaCompass.
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