EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI HUNGARY Ltd. Budapest HU
02 1EVERLIGHT CHEMICAL INDUSTRIAL CORPORATION Taipei TW
01 2Alprostadil
01 1France
02 1Taiwan
01 2Valid
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 2015-302 - Rev 00
Status : Valid
Issue Date : 2022-01-31
Type : Chemical
Substance Number : 1488
Certificate Number : R1-CEP 2012-204 - Rev 01
Status : Valid
Issue Date : 2022-06-27
Type : Chemical
Substance Number : 1488
A Prostaglandin E1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prostaglandin E1, including repackagers and relabelers. The FDA regulates Prostaglandin E1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prostaglandin E1 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 Prostaglandin E1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prostaglandin E1 supplier is an individual or a company that provides Prostaglandin E1 active pharmaceutical ingredient (API) or Prostaglandin E1 finished formulations upon request. The Prostaglandin E1 suppliers may include Prostaglandin E1 API manufacturers, exporters, distributors and traders.
click here to find a list of Prostaglandin E1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prostaglandin E1 CEP of the European Pharmacopoeia monograph is often referred to as a Prostaglandin E1 Certificate of Suitability (COS). The purpose of a Prostaglandin E1 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prostaglandin E1 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prostaglandin E1 to their clients by showing that a Prostaglandin E1 CEP has been issued for it. The manufacturer submits a Prostaglandin E1 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prostaglandin E1 CEP holder for the record. Additionally, the data presented in the Prostaglandin E1 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prostaglandin E1 DMF.
A Prostaglandin E1 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prostaglandin E1 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 Prostaglandin E1 suppliers with CEP (COS) on PharmaCompass.
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