Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
01 1Chlorambucil
01 1India
01 1Valid
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : CEP 2017-136 - Rev 01
Status : Valid
Issue Date : 2024-02-22
Type : Chemical
Substance Number : 137
88
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A CCG-39872 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCG-39872, including repackagers and relabelers. The FDA regulates CCG-39872 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCG-39872 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 CCG-39872 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CCG-39872 supplier is an individual or a company that provides CCG-39872 active pharmaceutical ingredient (API) or CCG-39872 finished formulations upon request. The CCG-39872 suppliers may include CCG-39872 API manufacturers, exporters, distributors and traders.
click here to find a list of CCG-39872 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A CCG-39872 CEP of the European Pharmacopoeia monograph is often referred to as a CCG-39872 Certificate of Suitability (COS). The purpose of a CCG-39872 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CCG-39872 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CCG-39872 to their clients by showing that a CCG-39872 CEP has been issued for it. The manufacturer submits a CCG-39872 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CCG-39872 CEP holder for the record. Additionally, the data presented in the CCG-39872 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CCG-39872 DMF.
A CCG-39872 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CCG-39872 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 CCG-39872 suppliers with CEP (COS) on PharmaCompass.
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