01 1XINJIANG NUZILINE BIO-PHARMACEUTICAL CO., LTD. Tuergen CN
01 1Estrogens, conjugated, 3.00% in lactose monohydrate
01 1China
01 1Valid
Estrogens, Conjugated, 3.00% In Lactose Monohydr...
Certificate Number : R1-CEP 2010-153 - Rev 00
Status : Valid
Issue Date : 2018-02-19
Type : Chemical
Substance Number : 1512
36
PharmaCompass offers a list of Conjugated Estrogens 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 Conjugated Estrogens manufacturer or Conjugated Estrogens supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Conjugated Estrogens manufacturer or Conjugated Estrogens supplier.
PharmaCompass also assists you with knowing the Conjugated Estrogens API Price utilized in the formulation of products. Conjugated Estrogens API Price is not always fixed or binding as the Conjugated Estrogens Price is obtained through a variety of data sources. The Conjugated Estrogens Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Par Estro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Par Estro, including repackagers and relabelers. The FDA regulates Par Estro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Par Estro 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 Par Estro manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Par Estro supplier is an individual or a company that provides Par Estro active pharmaceutical ingredient (API) or Par Estro finished formulations upon request. The Par Estro suppliers may include Par Estro API manufacturers, exporters, distributors and traders.
click here to find a list of Par Estro suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Par Estro CEP of the European Pharmacopoeia monograph is often referred to as a Par Estro Certificate of Suitability (COS). The purpose of a Par Estro CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Par Estro EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Par Estro to their clients by showing that a Par Estro CEP has been issued for it. The manufacturer submits a Par Estro CEP (COS) as part of the market authorization procedure, and it takes on the role of a Par Estro CEP holder for the record. Additionally, the data presented in the Par Estro CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Par Estro DMF.
A Par Estro CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Par Estro 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 Par Estro suppliers with CEP (COS) on PharmaCompass.
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