EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI HUNGARY Ltd. Budapest HU
02 1PHARMACIA & UPJOHN COMPANY LLC Kalamazoo US
01 2Dinoprost trometamol
01 1France
02 1U.S.A
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 : R0-CEP 2021-310 - Rev 00
Status : Valid
Issue Date : 2023-02-06
Type : Chemical
Substance Number : 1312
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Certificate Number : CEP 2016-337 - Rev 01
Status : Valid
Issue Date : 2024-01-09
Type : Chemical
Substance Number : 1312
A Dinoprost Tromethamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dinoprost Tromethamine, including repackagers and relabelers. The FDA regulates Dinoprost Tromethamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dinoprost Tromethamine 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 Dinoprost Tromethamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dinoprost Tromethamine supplier is an individual or a company that provides Dinoprost Tromethamine active pharmaceutical ingredient (API) or Dinoprost Tromethamine finished formulations upon request. The Dinoprost Tromethamine suppliers may include Dinoprost Tromethamine API manufacturers, exporters, distributors and traders.
click here to find a list of Dinoprost Tromethamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dinoprost Tromethamine CEP of the European Pharmacopoeia monograph is often referred to as a Dinoprost Tromethamine Certificate of Suitability (COS). The purpose of a Dinoprost Tromethamine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dinoprost Tromethamine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dinoprost Tromethamine to their clients by showing that a Dinoprost Tromethamine CEP has been issued for it. The manufacturer submits a Dinoprost Tromethamine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dinoprost Tromethamine CEP holder for the record. Additionally, the data presented in the Dinoprost Tromethamine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dinoprost Tromethamine DMF.
A Dinoprost Tromethamine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dinoprost Tromethamine 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 Dinoprost Tromethamine suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Dinoprost Tromethamine
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