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01 1JUNGBUNZLAUER LADENBURG GMBH Ladenburg DE
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01 1Citric acid, non-micronised and micronised
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01 1Switzerland
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01 1Valid
Citric Acid, Non-micronised And Micronised
Certificate Number : CEP 2016-005 - Rev 03
Status : Valid
Issue Date : 2025-01-23
Type : Chemical
Substance Number : 455
41
PharmaCompass offers a list of Citric Acid 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 Citric Acid manufacturer or Citric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Citric Acid manufacturer or Citric Acid supplier.
PharmaCompass also assists you with knowing the Citric Acid API Price utilized in the formulation of products. Citric Acid API Price is not always fixed or binding as the Citric Acid Price is obtained through a variety of data sources. The Citric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Uralyt U manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uralyt U, including repackagers and relabelers. The FDA regulates Uralyt U manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uralyt U 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 Uralyt U supplier is an individual or a company that provides Uralyt U active pharmaceutical ingredient (API) or Uralyt U finished formulations upon request. The Uralyt U suppliers may include Uralyt U API manufacturers, exporters, distributors and traders.
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A Uralyt U CEP of the European Pharmacopoeia monograph is often referred to as a Uralyt U Certificate of Suitability (COS). The purpose of a Uralyt U CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Uralyt U EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Uralyt U to their clients by showing that a Uralyt U CEP has been issued for it. The manufacturer submits a Uralyt U CEP (COS) as part of the market authorization procedure, and it takes on the role of a Uralyt U CEP holder for the record. Additionally, the data presented in the Uralyt U CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Uralyt U DMF.
A Uralyt U CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Uralyt U 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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