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 1LUSOCHIMICA S.P.A. Lomagna IT
03 1SIEGFRIED LTD Zofingen CH
04 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
01 4Nimodipine
01 1India
02 1Italy
03 1Spain
04 1Switzerland
01 3Valid
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 : R0-CEP 2020-353 - Rev 00
Status : Valid
Issue Date : 2022-10-25
Type : Chemical
Substance Number : 1245
Certificate Number : CEP 2022-403 - Rev 00
Status : Valid
Issue Date : 2024-01-24
Type : Chemical
Substance Number : 1245
Certificate Number : R0-CEP 1999-105 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2004-12-06
Type : Chemical
Substance Number : 1245
Certificate Number : CEP 2004-272 - Rev 03
Status : Valid
Issue Date : 2023-10-04
Type : Chemical
Substance Number : 1245
22
PharmaCompass offers a list of Nimodipine 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 Nimodipine manufacturer or Nimodipine supplier for your needs.
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A MolPort-001-840-190 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-840-190, including repackagers and relabelers. The FDA regulates MolPort-001-840-190 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-840-190 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 MolPort-001-840-190 supplier is an individual or a company that provides MolPort-001-840-190 active pharmaceutical ingredient (API) or MolPort-001-840-190 finished formulations upon request. The MolPort-001-840-190 suppliers may include MolPort-001-840-190 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-840-190 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-840-190 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-840-190 Certificate of Suitability (COS). The purpose of a MolPort-001-840-190 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-840-190 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-840-190 to their clients by showing that a MolPort-001-840-190 CEP has been issued for it. The manufacturer submits a MolPort-001-840-190 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-840-190 CEP holder for the record. Additionally, the data presented in the MolPort-001-840-190 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-840-190 DMF.
A MolPort-001-840-190 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-840-190 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 MolPort-001-840-190 suppliers with CEP (COS) on PharmaCompass.
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