Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
02 1CILAG AG Schaffhausen CH
03 1HUBEI BIOCAUSE HEILEN PHARMACEUTICAL CO., LTD. Jingmen City CN
04 1LIPOMED AG Arlesheim CH
05 1MSN LABORATORIES PRIVATE LIMITED Kardanur Village IN
06 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
07 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 7Cladribine
01 2China
02 2India
03 2Switzerland
04 1Taiwan
01 6Valid
02 1Withdrawn by Holder
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 2022-078 - Rev 00
Status : Valid
Issue Date : 2024-06-03
Type : Chemical
Substance Number : 2174
Certificate Number : R0-CEP 2020-049 - Rev 00
Status : Valid
Issue Date : 2021-08-20
Type : Chemical
Substance Number : 2174
Certificate Number : CEP 2023-104 - Rev 00
Status : Valid
Issue Date : 2024-04-22
Type : Chemical
Substance Number : 2174
Certificate Number : CEP 2022-076 - Rev 00
Status : Valid
Issue Date : 2024-04-05
Type : Chemical
Substance Number : 2174
Certificate Number : R0-CEP 2021-217 - Rev 01
Status : Valid
Issue Date : 2023-08-11
Type : Chemical
Substance Number : 2174
Certificate Number : CEP 2016-315 - Rev 01
Status : Valid
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2174
Certificate Number : R0-CEP 2012-132 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2014-10-29
Type : Chemical
Substance Number : 2174
A Cladribine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cladribine, including repackagers and relabelers. The FDA regulates Cladribine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cladribine 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 Cladribine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cladribine supplier is an individual or a company that provides Cladribine active pharmaceutical ingredient (API) or Cladribine finished formulations upon request. The Cladribine suppliers may include Cladribine API manufacturers, exporters, distributors and traders.
click here to find a list of Cladribine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cladribine CEP of the European Pharmacopoeia monograph is often referred to as a Cladribine Certificate of Suitability (COS). The purpose of a Cladribine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cladribine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cladribine to their clients by showing that a Cladribine CEP has been issued for it. The manufacturer submits a Cladribine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cladribine CEP holder for the record. Additionally, the data presented in the Cladribine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cladribine DMF.
A Cladribine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cladribine 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 Cladribine suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering Cladribine
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
