01 1EVERZINC NEDERLAND B.V. Eijsden NL
02 1EVERZINC St-Hyacinthe CA
03 1GRILLO ZINC POWDER GMBH Goslar DE
01 3Zinc oxide
01 2Belgium
02 1Germany
01 3Valid
Certificate Number : R1-CEP 2017-015 - Rev 00
Status : Valid
Issue Date : 2023-07-31
Type : Chemical
Substance Number : 252
Certificate Number : R1-CEP 2012-347 - Rev 01
Status : Valid
Issue Date : 2022-04-13
Type : Chemical
Substance Number : 252
Certificate Number : CEP 2018-254 - Rev 02
Status : Valid
Issue Date : 2025-01-29
Type : Chemical
Substance Number : 252
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PharmaCompass offers a list of Zinc Oxide 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 Zinc Oxide manufacturer or Zinc Oxide supplier for your needs.
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PharmaCompass also assists you with knowing the Zinc Oxide API Price utilized in the formulation of products. Zinc Oxide API Price is not always fixed or binding as the Zinc Oxide Price is obtained through a variety of data sources. The Zinc Oxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A XX 601 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of XX 601, including repackagers and relabelers. The FDA regulates XX 601 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. XX 601 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 XX 601 supplier is an individual or a company that provides XX 601 active pharmaceutical ingredient (API) or XX 601 finished formulations upon request. The XX 601 suppliers may include XX 601 API manufacturers, exporters, distributors and traders.
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A XX 601 CEP of the European Pharmacopoeia monograph is often referred to as a XX 601 Certificate of Suitability (COS). The purpose of a XX 601 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of XX 601 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of XX 601 to their clients by showing that a XX 601 CEP has been issued for it. The manufacturer submits a XX 601 CEP (COS) as part of the market authorization procedure, and it takes on the role of a XX 601 CEP holder for the record. Additionally, the data presented in the XX 601 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the XX 601 DMF.
A XX 601 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. XX 601 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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