01 2JIANGSU DINGYE PHARMACEUTICAL CO.,LTD Funing County CN
02 1KAIFENG MINGREN PHARMACEUTICAL CO., LTD. Kaifeng CN
03 2MICRO LABS LIMITED Bengaluru IN
04 2SHOUGUANG FUKANG PHARMACEUTICAL CO., LTD. Shouguang City CN
01 2Phloroglucinol
02 4Phloroglucinol dihydrate
03 1Phloroglucinol dihydrate, Process-II
01 5China
02 2India
01 7Valid
Certificate Number : CEP 2018-002 - Rev 01
Status : Valid
Issue Date : 2024-08-26
Type : Chemical
Substance Number : 2302
Certificate Number : CEP 2018-003 - Rev 01
Status : Valid
Issue Date : 2024-08-26
Type : Chemical
Substance Number : 2301
Certificate Number : R1-CEP 2016-273 - Rev 00
Status : Valid
Issue Date : 2022-03-08
Type : Chemical
Substance Number : 2302
Certificate Number : R0-CEP 2020-223 - Rev 00
Status : Valid
Issue Date : 2022-03-31
Type : Chemical
Substance Number : 2302
Phloroglucinol Dihydrate, Process-II
Certificate Number : CEP 2024-444 - Rev 00
Status : Valid
Issue Date : 2024-11-21
Type : Chemical
Substance Number : 2302
Certificate Number : R1-CEP 2016-007 - Rev 00
Status : Valid
Issue Date : 2021-10-22
Type : Chemical
Substance Number : 2301
Certificate Number : R1-CEP 2013-099 - Rev 01
Status : Valid
Issue Date : 2022-10-06
Type : Chemical
Substance Number : 2302
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A cyclohexa-1,3,5-triene-1,3,5-triol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of cyclohexa-1,3,5-triene-1,3,5-triol, including repackagers and relabelers. The FDA regulates cyclohexa-1,3,5-triene-1,3,5-triol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. cyclohexa-1,3,5-triene-1,3,5-triol 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 cyclohexa-1,3,5-triene-1,3,5-triol supplier is an individual or a company that provides cyclohexa-1,3,5-triene-1,3,5-triol active pharmaceutical ingredient (API) or cyclohexa-1,3,5-triene-1,3,5-triol finished formulations upon request. The cyclohexa-1,3,5-triene-1,3,5-triol suppliers may include cyclohexa-1,3,5-triene-1,3,5-triol API manufacturers, exporters, distributors and traders.
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A cyclohexa-1,3,5-triene-1,3,5-triol CEP of the European Pharmacopoeia monograph is often referred to as a cyclohexa-1,3,5-triene-1,3,5-triol Certificate of Suitability (COS). The purpose of a cyclohexa-1,3,5-triene-1,3,5-triol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of cyclohexa-1,3,5-triene-1,3,5-triol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of cyclohexa-1,3,5-triene-1,3,5-triol to their clients by showing that a cyclohexa-1,3,5-triene-1,3,5-triol CEP has been issued for it. The manufacturer submits a cyclohexa-1,3,5-triene-1,3,5-triol CEP (COS) as part of the market authorization procedure, and it takes on the role of a cyclohexa-1,3,5-triene-1,3,5-triol CEP holder for the record. Additionally, the data presented in the cyclohexa-1,3,5-triene-1,3,5-triol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the cyclohexa-1,3,5-triene-1,3,5-triol DMF.
A cyclohexa-1,3,5-triene-1,3,5-triol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. cyclohexa-1,3,5-triene-1,3,5-triol 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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