01 1MAC CHEM PRODUCTS (INDIA) PVT. LTD. Mumbai IN
02 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
03 1TAKEDA GMBH Konstanz DE
01 3Suxamethonium Chloride
01 2India
02 1Japan
01 3Valid
Certificate Number : CEP 2012-025 - Rev 03
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 248
Certificate Number : CEP 2013-210 - Rev 01
Status : Valid
Issue Date : 2024-05-30
Type : Chemical
Substance Number : 248
Certificate Number : R2-CEP 1995-021 - Rev 10
Status : Valid
Issue Date : 2023-08-11
Type : Chemical
Substance Number : 248
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PharmaCompass offers a list of Succinylcholine Chloride 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 Succinylcholine Chloride manufacturer or Succinylcholine Chloride supplier for your needs.
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A Scoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Scoline, including repackagers and relabelers. The FDA regulates Scoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Scoline 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 Scoline supplier is an individual or a company that provides Scoline active pharmaceutical ingredient (API) or Scoline finished formulations upon request. The Scoline suppliers may include Scoline API manufacturers, exporters, distributors and traders.
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A Scoline CEP of the European Pharmacopoeia monograph is often referred to as a Scoline Certificate of Suitability (COS). The purpose of a Scoline CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Scoline EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Scoline to their clients by showing that a Scoline CEP has been issued for it. The manufacturer submits a Scoline CEP (COS) as part of the market authorization procedure, and it takes on the role of a Scoline CEP holder for the record. Additionally, the data presented in the Scoline CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Scoline DMF.
A Scoline CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Scoline CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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