01 1VENATOR GERMANY GMBH Duisburg DE
01 1Barium sulfate
01 1U.S.A
01 1Valid
Certificate Number : R1-CEP 2006-257 - Rev 04
Status : Valid
Issue Date : 2021-09-29
Type : Chemical
Substance Number : 10
68
PharmaCompass offers a list of Barium Sulfate 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 Barium Sulfate manufacturer or Barium Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Barium Sulfate API Price utilized in the formulation of products. Barium Sulfate API Price is not always fixed or binding as the Barium Sulfate Price is obtained through a variety of data sources. The Barium Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EZCAT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EZCAT, including repackagers and relabelers. The FDA regulates EZCAT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EZCAT 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 EZCAT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EZCAT supplier is an individual or a company that provides EZCAT active pharmaceutical ingredient (API) or EZCAT finished formulations upon request. The EZCAT suppliers may include EZCAT API manufacturers, exporters, distributors and traders.
click here to find a list of EZCAT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EZCAT CEP of the European Pharmacopoeia monograph is often referred to as a EZCAT Certificate of Suitability (COS). The purpose of a EZCAT CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of EZCAT EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of EZCAT to their clients by showing that a EZCAT CEP has been issued for it. The manufacturer submits a EZCAT CEP (COS) as part of the market authorization procedure, and it takes on the role of a EZCAT CEP holder for the record. Additionally, the data presented in the EZCAT CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the EZCAT DMF.
A EZCAT CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. EZCAT 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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