Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1OLPHA AS Olaine LV
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.
Certificate Number : CEP 2017-284 - Rev 03
Status : Valid
Issue Date : 2024-10-28
Type : Chemical
Substance Number : 463
76
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A adamantan-1-amine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of adamantan-1-amine hydrochloride, including repackagers and relabelers. The FDA regulates adamantan-1-amine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. adamantan-1-amine hydrochloride 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 adamantan-1-amine hydrochloride supplier is an individual or a company that provides adamantan-1-amine hydrochloride active pharmaceutical ingredient (API) or adamantan-1-amine hydrochloride finished formulations upon request. The adamantan-1-amine hydrochloride suppliers may include adamantan-1-amine hydrochloride API manufacturers, exporters, distributors and traders.
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A adamantan-1-amine hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a adamantan-1-amine hydrochloride Certificate of Suitability (COS). The purpose of a adamantan-1-amine hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of adamantan-1-amine hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of adamantan-1-amine hydrochloride to their clients by showing that a adamantan-1-amine hydrochloride CEP has been issued for it. The manufacturer submits a adamantan-1-amine hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a adamantan-1-amine hydrochloride CEP holder for the record. Additionally, the data presented in the adamantan-1-amine hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the adamantan-1-amine hydrochloride DMF.
A adamantan-1-amine hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. adamantan-1-amine hydrochloride 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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