01 1BIOSPECTRA, INC. Bangor US
01 1Potassium bromide
01 1U.S.A
01 1Valid
Certificate Number : CEP 2022-224 - Rev 00
Status : Valid
Issue Date : 2024-05-24
Type : Chemical
Substance Number : 184
84
PharmaCompass offers a list of Potassium Bromide 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 Potassium Bromide manufacturer or Potassium Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Potassium Bromide API Price utilized in the formulation of products. Potassium Bromide API Price is not always fixed or binding as the Potassium Bromide Price is obtained through a variety of data sources. The Potassium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KBr manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KBr, including repackagers and relabelers. The FDA regulates KBr manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KBr 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 KBr manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KBr supplier is an individual or a company that provides KBr active pharmaceutical ingredient (API) or KBr finished formulations upon request. The KBr suppliers may include KBr API manufacturers, exporters, distributors and traders.
click here to find a list of KBr suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KBr CEP of the European Pharmacopoeia monograph is often referred to as a KBr Certificate of Suitability (COS). The purpose of a KBr CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of KBr EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of KBr to their clients by showing that a KBr CEP has been issued for it. The manufacturer submits a KBr CEP (COS) as part of the market authorization procedure, and it takes on the role of a KBr CEP holder for the record. Additionally, the data presented in the KBr CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the KBr DMF.
A KBr CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. KBr 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 KBr suppliers with CEP (COS) on PharmaCompass.
