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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A 1-Adamantanamine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1-Adamantanamine HCl, including repackagers and relabelers. The FDA regulates 1-Adamantanamine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1-Adamantanamine HCl 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 1-Adamantanamine HCl supplier is an individual or a company that provides 1-Adamantanamine HCl active pharmaceutical ingredient (API) or 1-Adamantanamine HCl finished formulations upon request. The 1-Adamantanamine HCl suppliers may include 1-Adamantanamine HCl API manufacturers, exporters, distributors and traders.
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A 1-Adamantanamine HCl CEP of the European Pharmacopoeia monograph is often referred to as a 1-Adamantanamine HCl Certificate of Suitability (COS). The purpose of a 1-Adamantanamine HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1-Adamantanamine HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1-Adamantanamine HCl to their clients by showing that a 1-Adamantanamine HCl CEP has been issued for it. The manufacturer submits a 1-Adamantanamine HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1-Adamantanamine HCl CEP holder for the record. Additionally, the data presented in the 1-Adamantanamine HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1-Adamantanamine HCl DMF.
A 1-Adamantanamine HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1-Adamantanamine HCl 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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