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 E160A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E160A, including repackagers and relabelers. The FDA regulates E160A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E160A 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 E160A manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E160A supplier is an individual or a company that provides E160A active pharmaceutical ingredient (API) or E160A finished formulations upon request. The E160A suppliers may include E160A API manufacturers, exporters, distributors and traders.
click here to find a list of E160A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E160A CEP of the European Pharmacopoeia monograph is often referred to as a E160A Certificate of Suitability (COS). The purpose of a E160A CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of E160A EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of E160A to their clients by showing that a E160A CEP has been issued for it. The manufacturer submits a E160A CEP (COS) as part of the market authorization procedure, and it takes on the role of a E160A CEP holder for the record. Additionally, the data presented in the E160A CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the E160A DMF.
A E160A CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. E160A 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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