Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 2Moehs Iberica S.L. Rubi ES
02 1Nycomed Austria GmbH Linz AT
01 3Celiprolol hydrochloride
01 1Austria
02 2Spain
01 1Valid
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 2007-220 - Rev 04
Status : Valid
Issue Date : 2024-03-08
Type : Chemical
Substance Number : 1632
Certificate Number : R0-CEP 2006-259 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2009-09-04
Type : Chemical
Substance Number : 1632
Certificate Number : R1-CEP 2004-294 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2013-10-11
Type : Chemical
Substance Number : 1632
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A Celiprolol clorhidrato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Celiprolol clorhidrato, including repackagers and relabelers. The FDA regulates Celiprolol clorhidrato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Celiprolol clorhidrato 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 Celiprolol clorhidrato supplier is an individual or a company that provides Celiprolol clorhidrato active pharmaceutical ingredient (API) or Celiprolol clorhidrato finished formulations upon request. The Celiprolol clorhidrato suppliers may include Celiprolol clorhidrato API manufacturers, exporters, distributors and traders.
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A Celiprolol clorhidrato CEP of the European Pharmacopoeia monograph is often referred to as a Celiprolol clorhidrato Certificate of Suitability (COS). The purpose of a Celiprolol clorhidrato CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Celiprolol clorhidrato EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Celiprolol clorhidrato to their clients by showing that a Celiprolol clorhidrato CEP has been issued for it. The manufacturer submits a Celiprolol clorhidrato CEP (COS) as part of the market authorization procedure, and it takes on the role of a Celiprolol clorhidrato CEP holder for the record. Additionally, the data presented in the Celiprolol clorhidrato CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Celiprolol clorhidrato DMF.
A Celiprolol clorhidrato CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Celiprolol clorhidrato 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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