01 1CHIFENG PHARMACEUTICAL CO., LTD. Chifeng CN
02 1Glaxo Wellcome London GB
01 2Griseofulvin
01 1China
02 1United Kingdom
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R0-CEP 2000-374 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2001-11-21
Type : TSE
Substance Number : 182
Certificate Number : R1-CEP 2002-143 - Rev 02
Status : Valid
Issue Date : 2022-11-07
Type : Chemical
Substance Number : 182
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PharmaCompass offers a list of Griseofulvin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Griseofulvin manufacturer or Griseofulvin supplier for your needs.
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A Greosin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Greosin, including repackagers and relabelers. The FDA regulates Greosin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Greosin 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 Greosin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Greosin supplier is an individual or a company that provides Greosin active pharmaceutical ingredient (API) or Greosin finished formulations upon request. The Greosin suppliers may include Greosin API manufacturers, exporters, distributors and traders.
click here to find a list of Greosin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Greosin CEP of the European Pharmacopoeia monograph is often referred to as a Greosin Certificate of Suitability (COS). The purpose of a Greosin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Greosin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Greosin to their clients by showing that a Greosin CEP has been issued for it. The manufacturer submits a Greosin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Greosin CEP holder for the record. Additionally, the data presented in the Greosin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Greosin DMF.
A Greosin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Greosin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Greosin suppliers with CEP (COS) on PharmaCompass.
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