Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1AREVIPHARMA GMBH Radebeul DE
03 1SIEGFRIED LTD. Zofingen CH
04 1Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. Hanzhong City CN
01 4Sotalol hydrochloride
01 1China
02 1Germany
03 1Spain
04 1Switzerland
01 2Valid
02 2Withdrawn by Holder
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 2002-049 - Rev 08
Status : Valid
Issue Date : 2024-03-12
Type : Chemical
Substance Number : 2004
Certificate Number : CEP 2005-154 - Rev 04
Status : Valid
Issue Date : 2024-02-20
Type : Chemical
Substance Number : 2004
Certificate Number : R1-CEP 2005-295 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2012-09-06
Type : Chemical
Substance Number : 2004
Certificate Number : R1-CEP 2003-196 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2014-09-12
Type : Chemical
Substance Number : 2004
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PharmaCompass offers a list of Sotalol Hydrochloride 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 Sotalol Hydrochloride manufacturer or Sotalol Hydrochloride supplier for your needs.
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A Sotylize manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sotylize, including repackagers and relabelers. The FDA regulates Sotylize manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sotylize 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 Sotylize supplier is an individual or a company that provides Sotylize active pharmaceutical ingredient (API) or Sotylize finished formulations upon request. The Sotylize suppliers may include Sotylize API manufacturers, exporters, distributors and traders.
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A Sotylize CEP of the European Pharmacopoeia monograph is often referred to as a Sotylize Certificate of Suitability (COS). The purpose of a Sotylize CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sotylize EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sotylize to their clients by showing that a Sotylize CEP has been issued for it. The manufacturer submits a Sotylize CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sotylize CEP holder for the record. Additionally, the data presented in the Sotylize CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sotylize DMF.
A Sotylize CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sotylize 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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