01 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
02 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
01 2Fluocinolone acetonide
01 2China
01 2Valid
Certificate Number : R0-CEP 2020-366 - Rev 00
Status : Valid
Issue Date : 2022-08-17
Type : Chemical
Substance Number : 494
Certificate Number : R0-CEP 2021-011 - Rev 00
Status : Valid
Issue Date : 2022-03-21
Type : Chemical
Substance Number : 494
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PharmaCompass offers a list of Fluocinolone Acetonide 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 Fluocinolone Acetonide manufacturer or Fluocinolone Acetonide supplier for your needs.
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A component of Neo-Synalar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of component of Neo-Synalar, including repackagers and relabelers. The FDA regulates component of Neo-Synalar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. component of Neo-Synalar 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 component of Neo-Synalar supplier is an individual or a company that provides component of Neo-Synalar active pharmaceutical ingredient (API) or component of Neo-Synalar finished formulations upon request. The component of Neo-Synalar suppliers may include component of Neo-Synalar API manufacturers, exporters, distributors and traders.
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A component of Neo-Synalar CEP of the European Pharmacopoeia monograph is often referred to as a component of Neo-Synalar Certificate of Suitability (COS). The purpose of a component of Neo-Synalar CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of component of Neo-Synalar EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of component of Neo-Synalar to their clients by showing that a component of Neo-Synalar CEP has been issued for it. The manufacturer submits a component of Neo-Synalar CEP (COS) as part of the market authorization procedure, and it takes on the role of a component of Neo-Synalar CEP holder for the record. Additionally, the data presented in the component of Neo-Synalar CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the component of Neo-Synalar DMF.
A component of Neo-Synalar CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. component of Neo-Synalar 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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