Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
01 1OLPHA AS Olaine LV
02 1Moehs Iberica S.L. Rubi ES
03 1ZHEJIANG APELOA KANGYU PHARMACEUTICAL CO., LTD. Jinhua CN
01 3Amantadine hydrochloride
01 1Latvia
02 1Spain
03 1Blank
01 3Valid
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
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
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Certificate Number : CEP 2025-139 - Rev 00
Status : Valid
Issue Date : 2026-05-22
Type : Chemical
Substance Number : 463
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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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, and more, enabling you to easily find the right Amantadine Hydrochloride manufacturer or Amantadine Hydrochloride supplier for your needs.
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A Virosol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Virosol, including repackagers and relabelers. The FDA regulates Virosol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Virosol 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 Virosol supplier is an individual or a company that provides Virosol active pharmaceutical ingredient (API) or Virosol finished formulations upon request. The Virosol suppliers may include Virosol API manufacturers, exporters, distributors and traders.
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A Virosol CEP of the European Pharmacopoeia monograph is often referred to as a Virosol Certificate of Suitability (COS). The purpose of a Virosol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Virosol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Virosol to their clients by showing that a Virosol CEP has been issued for it. The manufacturer submits a Virosol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Virosol CEP holder for the record. Additionally, the data presented in the Virosol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Virosol DMF.
A Virosol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Virosol 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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