Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1PCAS Ecully FR
02 1MENADIONA, S.L. Palafolls ES
01 2Clomifene citrate
01 1France
02 1Spain
01 1Suspended by EDQM GMP non-compliance
02 1Valid
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Certificate Number : R1-CEP 2003-251 - Rev 06
Status : Valid
Issue Date : 2022-02-09
Type : Chemical
Substance Number : 997
Certificate Number : R1-CEP 2003-193 - Rev 04
Status : Suspended by EDQM GMP non-compliance
Issue Date : 2020-08-07
Type : Chemical
Substance Number : 997
A Clomiphene Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clomiphene Citrate, including repackagers and relabelers. The FDA regulates Clomiphene Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clomiphene Citrate 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 Clomiphene Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clomiphene Citrate supplier is an individual or a company that provides Clomiphene Citrate active pharmaceutical ingredient (API) or Clomiphene Citrate finished formulations upon request. The Clomiphene Citrate suppliers may include Clomiphene Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Clomiphene Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clomiphene Citrate CEP of the European Pharmacopoeia monograph is often referred to as a Clomiphene Citrate Certificate of Suitability (COS). The purpose of a Clomiphene Citrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clomiphene Citrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clomiphene Citrate to their clients by showing that a Clomiphene Citrate CEP has been issued for it. The manufacturer submits a Clomiphene Citrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clomiphene Citrate CEP holder for the record. Additionally, the data presented in the Clomiphene Citrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clomiphene Citrate DMF.
A Clomiphene Citrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clomiphene Citrate 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 Clomiphene Citrate suppliers with CEP (COS) on PharmaCompass.
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