Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1PHARMACIA & UPJOHN COMPANY LLC Kalamazoo US
02 1EUROAPI FRANCE Vertolaye FR
03 1CURIA SPAIN S.A.U. Boecillo ES
04 1SM BIOMED SDN BHD Sungai Petani MY
05 1SYMBIOTICA SPECIALITY INGREDIENTS SDN. BHD. Perai MY
06 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
07 1XI’AN GUOKANG RUIJIN PHARMACEUTICAL CO., LTD. Xi’an City CN
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
Dexamethasone Sodium Phosphate
Certificate Number : R1-CEP 1998-154 - Rev 06
Status : Valid
Issue Date : 2021-07-07
Type : Chemical
Substance Number : 549
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Dexamethasone Sodium Phosphate
Certificate Number : R2-CEP 1992-014 - Rev 07
Status : Valid
Issue Date : 2021-12-16
Type : Chemical
Substance Number : 549
86
PharmaCompass offers a list of Dexamethasone Sodium Phosphate 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 Dexamethasone Sodium Phosphate manufacturer or Dexamethasone Sodium Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dexamethasone Sodium Phosphate manufacturer or Dexamethasone Sodium Phosphate supplier.
PharmaCompass also assists you with knowing the Dexamethasone Sodium Phosphate API Price utilized in the formulation of products. Dexamethasone Sodium Phosphate API Price is not always fixed or binding as the Dexamethasone Sodium Phosphate Price is obtained through a variety of data sources. The Dexamethasone Sodium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KS-1150 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KS-1150, including repackagers and relabelers. The FDA regulates KS-1150 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KS-1150 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 KS-1150 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KS-1150 supplier is an individual or a company that provides KS-1150 active pharmaceutical ingredient (API) or KS-1150 finished formulations upon request. The KS-1150 suppliers may include KS-1150 API manufacturers, exporters, distributors and traders.
click here to find a list of KS-1150 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KS-1150 CEP of the European Pharmacopoeia monograph is often referred to as a KS-1150 Certificate of Suitability (COS). The purpose of a KS-1150 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of KS-1150 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of KS-1150 to their clients by showing that a KS-1150 CEP has been issued for it. The manufacturer submits a KS-1150 CEP (COS) as part of the market authorization procedure, and it takes on the role of a KS-1150 CEP holder for the record. Additionally, the data presented in the KS-1150 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the KS-1150 DMF.
A KS-1150 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. KS-1150 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 KS-1150 suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering KS-1150
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