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 Kaliumbromid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kaliumbromid, including repackagers and relabelers. The FDA regulates Kaliumbromid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kaliumbromid API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Kaliumbromid supplier is an individual or a company that provides Kaliumbromid active pharmaceutical ingredient (API) or Kaliumbromid finished formulations upon request. The Kaliumbromid suppliers may include Kaliumbromid API manufacturers, exporters, distributors and traders.
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A Kaliumbromid CEP of the European Pharmacopoeia monograph is often referred to as a Kaliumbromid Certificate of Suitability (COS). The purpose of a Kaliumbromid CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Kaliumbromid EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Kaliumbromid to their clients by showing that a Kaliumbromid CEP has been issued for it. The manufacturer submits a Kaliumbromid CEP (COS) as part of the market authorization procedure, and it takes on the role of a Kaliumbromid CEP holder for the record. Additionally, the data presented in the Kaliumbromid CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Kaliumbromid DMF.
A Kaliumbromid CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Kaliumbromid CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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