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
70
PharmaCompass offers a list of Chlorambucil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Chlorambucil manufacturer or Chlorambucil supplier for your needs.
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PharmaCompass also assists you with knowing the Chlorambucil API Price utilized in the formulation of products. Chlorambucil API Price is not always fixed or binding as the Chlorambucil Price is obtained through a variety of data sources. The Chlorambucil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Leukeran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Leukeran, including repackagers and relabelers. The FDA regulates Leukeran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Leukeran API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Leukeran supplier is an individual or a company that provides Leukeran active pharmaceutical ingredient (API) or Leukeran finished formulations upon request. The Leukeran suppliers may include Leukeran API manufacturers, exporters, distributors and traders.
click here to find a list of Leukeran suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Leukeran CEP of the European Pharmacopoeia monograph is often referred to as a Leukeran Certificate of Suitability (COS). The purpose of a Leukeran CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Leukeran EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Leukeran to their clients by showing that a Leukeran CEP has been issued for it. The manufacturer submits a Leukeran CEP (COS) as part of the market authorization procedure, and it takes on the role of a Leukeran CEP holder for the record. Additionally, the data presented in the Leukeran CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Leukeran DMF.
A Leukeran CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Leukeran 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 Leukeran suppliers with CEP (COS) on PharmaCompass.
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