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 NSC 3088 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NSC 3088, including repackagers and relabelers. The FDA regulates NSC 3088 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NSC 3088 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 NSC 3088 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A NSC 3088 supplier is an individual or a company that provides NSC 3088 active pharmaceutical ingredient (API) or NSC 3088 finished formulations upon request. The NSC 3088 suppliers may include NSC 3088 API manufacturers, exporters, distributors and traders.
click here to find a list of NSC 3088 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A NSC 3088 CEP of the European Pharmacopoeia monograph is often referred to as a NSC 3088 Certificate of Suitability (COS). The purpose of a NSC 3088 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NSC 3088 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NSC 3088 to their clients by showing that a NSC 3088 CEP has been issued for it. The manufacturer submits a NSC 3088 CEP (COS) as part of the market authorization procedure, and it takes on the role of a NSC 3088 CEP holder for the record. Additionally, the data presented in the NSC 3088 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NSC 3088 DMF.
A NSC 3088 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NSC 3088 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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