01 1Becton, Dickinson and Company Sparks US
02 1HA1 NATURAL LIMITED Greenock GB
01 1Animal Charcoal
02 1Charcoal Agar, (Product code 289410)
01 2U.S.A
01 2Valid
Charcoal Agar, (Product Code 289410)
Certificate Number : R1-CEP 2000-285 - Rev 02
Status : Valid
Issue Date : 2011-04-15
Type : TSE
Substance Number :
Certificate Number : R1-CEP 2003-003 - Rev 01
Status : Valid
Issue Date : 2012-05-07
Type : TSE
Substance Number :
96
PharmaCompass offers a list of Carbon 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 Carbon manufacturer or Carbon supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carbon manufacturer or Carbon supplier.
A C manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C, including repackagers and relabelers. The FDA regulates C manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C 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 C manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A C supplier is an individual or a company that provides C active pharmaceutical ingredient (API) or C finished formulations upon request. The C suppliers may include C API manufacturers, exporters, distributors and traders.
click here to find a list of C suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A C CEP of the European Pharmacopoeia monograph is often referred to as a C Certificate of Suitability (COS). The purpose of a C CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of C EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of C to their clients by showing that a C CEP has been issued for it. The manufacturer submits a C CEP (COS) as part of the market authorization procedure, and it takes on the role of a C CEP holder for the record. Additionally, the data presented in the C CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the C DMF.
A C CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. C 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 C suppliers with CEP (COS) on PharmaCompass.
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