01 1DSM Nutritional Products Ltd. Kaiseraugst CH
01 1Betacarotene
01 1U.S.A
01 1Valid
Certificate Number : R1-CEP 2010-383 - Rev 01
Status : Valid
Issue Date : 2019-06-14
Type : Chemical
Substance Number : 1069
69
PharmaCompass offers a list of Beta Carotene 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 Beta Carotene manufacturer or Beta Carotene supplier for your needs.
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PharmaCompass also assists you with knowing the Beta Carotene API Price utilized in the formulation of products. Beta Carotene API Price is not always fixed or binding as the Beta Carotene Price is obtained through a variety of data sources. The Beta Carotene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CI 40800 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI 40800, including repackagers and relabelers. The FDA regulates CI 40800 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI 40800 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 CI 40800 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CI 40800 supplier is an individual or a company that provides CI 40800 active pharmaceutical ingredient (API) or CI 40800 finished formulations upon request. The CI 40800 suppliers may include CI 40800 API manufacturers, exporters, distributors and traders.
click here to find a list of CI 40800 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CI 40800 CEP of the European Pharmacopoeia monograph is often referred to as a CI 40800 Certificate of Suitability (COS). The purpose of a CI 40800 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CI 40800 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CI 40800 to their clients by showing that a CI 40800 CEP has been issued for it. The manufacturer submits a CI 40800 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CI 40800 CEP holder for the record. Additionally, the data presented in the CI 40800 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CI 40800 DMF.
A CI 40800 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CI 40800 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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