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 Aman manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aman, including repackagers and relabelers. The FDA regulates Aman manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aman 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 Aman supplier is an individual or a company that provides Aman active pharmaceutical ingredient (API) or Aman finished formulations upon request. The Aman suppliers may include Aman API manufacturers, exporters, distributors and traders.
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A Aman CEP of the European Pharmacopoeia monograph is often referred to as a Aman Certificate of Suitability (COS). The purpose of a Aman CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aman EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aman to their clients by showing that a Aman CEP has been issued for it. The manufacturer submits a Aman CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aman CEP holder for the record. Additionally, the data presented in the Aman CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aman DMF.
A Aman CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aman 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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