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Status : Withdrawn by Holder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
A GRISEOFULVIN, ULTRAMICROSIZE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GRISEOFULVIN, ULTRAMICROSIZE, including repackagers and relabelers. The FDA regulates GRISEOFULVIN, ULTRAMICROSIZE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GRISEOFULVIN, ULTRAMICROSIZE 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 GRISEOFULVIN, ULTRAMICROSIZE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A GRISEOFULVIN, ULTRAMICROSIZE supplier is an individual or a company that provides GRISEOFULVIN, ULTRAMICROSIZE active pharmaceutical ingredient (API) or GRISEOFULVIN, ULTRAMICROSIZE finished formulations upon request. The GRISEOFULVIN, ULTRAMICROSIZE suppliers may include GRISEOFULVIN, ULTRAMICROSIZE API manufacturers, exporters, distributors and traders.
click here to find a list of GRISEOFULVIN, ULTRAMICROSIZE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A GRISEOFULVIN, ULTRAMICROSIZE CEP of the European Pharmacopoeia monograph is often referred to as a GRISEOFULVIN, ULTRAMICROSIZE Certificate of Suitability (COS). The purpose of a GRISEOFULVIN, ULTRAMICROSIZE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of GRISEOFULVIN, ULTRAMICROSIZE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of GRISEOFULVIN, ULTRAMICROSIZE to their clients by showing that a GRISEOFULVIN, ULTRAMICROSIZE CEP has been issued for it. The manufacturer submits a GRISEOFULVIN, ULTRAMICROSIZE CEP (COS) as part of the market authorization procedure, and it takes on the role of a GRISEOFULVIN, ULTRAMICROSIZE CEP holder for the record. Additionally, the data presented in the GRISEOFULVIN, ULTRAMICROSIZE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the GRISEOFULVIN, ULTRAMICROSIZE DMF.
A GRISEOFULVIN, ULTRAMICROSIZE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. GRISEOFULVIN, ULTRAMICROSIZE 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 GRISEOFULVIN, ULTRAMICROSIZE suppliers with CEP (COS) on PharmaCompass.
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