Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1OLPHA AS Olaine LV
01 2Amantadine hydrochloride
01 1Latvia
02 1Spain
01 2Valid
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 : R1-CEP 2000-014 - Rev 08
Status : Valid
Issue Date : 2023-05-25
Type : Chemical
Substance Number : 463
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
Certificate Number : CEP 2017-284 - Rev 03
Status : Valid
Issue Date : 2024-10-28
Type : Chemical
Substance Number : 463
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PharmaCompass offers a list of Amantadine 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 Amantadine Hydrochloride manufacturer or Amantadine Hydrochloride supplier for your needs.
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A Viregyt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Viregyt, including repackagers and relabelers. The FDA regulates Viregyt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Viregyt 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 Viregyt supplier is an individual or a company that provides Viregyt active pharmaceutical ingredient (API) or Viregyt finished formulations upon request. The Viregyt suppliers may include Viregyt API manufacturers, exporters, distributors and traders.
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A Viregyt CEP of the European Pharmacopoeia monograph is often referred to as a Viregyt Certificate of Suitability (COS). The purpose of a Viregyt CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Viregyt EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Viregyt to their clients by showing that a Viregyt CEP has been issued for it. The manufacturer submits a Viregyt CEP (COS) as part of the market authorization procedure, and it takes on the role of a Viregyt CEP holder for the record. Additionally, the data presented in the Viregyt CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Viregyt DMF.
A Viregyt CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Viregyt 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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