Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
01 2EGIS Pharmaceuticals PLC Budapest HU
02 1EUROAPI FRANCE Vertolaye FR
03 1COHANCE LIFESCIENCES LIMITED Mumbai IN
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Certificate Number : R1-CEP 1997-058 - Rev 06
Status : Valid
Issue Date : 2023-03-20
Type : Chemical
Substance Number : 925
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 2002-218 - Rev 05
Status : Valid
Issue Date : 2023-02-07
Type : Chemical
Substance Number : 925
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2018-144 - Rev 05
Status : Valid
Issue Date : 2025-06-05
Type : Chemical
Substance Number : 925
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Levomepromazine Maleate, Process 2
Certificate Number : R1-CEP 2016-215 - Rev 01
Status : Valid
Issue Date : 2023-03-31
Type : Chemical
Substance Number : 925
69
PharmaCompass offers a list of Levomepromazine Maleate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Levomepromazine Maleate manufacturer or Levomepromazine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levomepromazine Maleate manufacturer or Levomepromazine Maleate supplier.
A Sofmin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sofmin, including repackagers and relabelers. The FDA regulates Sofmin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sofmin 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 Sofmin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sofmin supplier is an individual or a company that provides Sofmin active pharmaceutical ingredient (API) or Sofmin finished formulations upon request. The Sofmin suppliers may include Sofmin API manufacturers, exporters, distributors and traders.
click here to find a list of Sofmin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Sofmin CEP of the European Pharmacopoeia monograph is often referred to as a Sofmin Certificate of Suitability (COS). The purpose of a Sofmin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sofmin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sofmin to their clients by showing that a Sofmin CEP has been issued for it. The manufacturer submits a Sofmin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sofmin CEP holder for the record. Additionally, the data presented in the Sofmin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sofmin DMF.
A Sofmin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sofmin 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 Sofmin suppliers with CEP (COS) on PharmaCompass.
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