Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 1EGIS Pharmaceuticals PLC Budapest HU
02 2TAPI NL B.V. Amsterdam NL
03 2ZHEJIANG CHIRAL MEDICINE CHEMICALS CO., LTD. Hangzhou CN
04 1ZHEJIANG WILD WIND PHARMACEUTICAL CO., LTD. Geshan Town CN
01 5Methyldopa
02 1Methyldopa, Process B
01 3China
02 1Hungary
03 2Blank
01 6Valid
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R1-CEP 1996-033 - Rev 07
Status : Valid
Issue Date : 2019-04-10
Type : Chemical
Substance Number : 45
Certificate Number : R1-CEP 2018-065 - Rev 00
Status : Valid
Issue Date : 2023-06-20
Type : Chemical
Substance Number : 45
Certificate Number : R1-CEP 2003-241 - Rev 03
Status : Valid
Issue Date : 2017-05-17
Type : Chemical
Substance Number : 45
Certificate Number : R1-CEP 2009-120 - Rev 01
Status : Valid
Issue Date : 2018-04-18
Type : Chemical
Substance Number : 45
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Certificate Number : CEP 2010-326 - Rev 06
Status : Valid
Issue Date : 2025-03-14
Type : Chemical
Substance Number : 45
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2010-182 - Rev 05
Status : Valid
Issue Date : 2025-03-18
Type : Chemical
Substance Number : 45
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
46
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A Aldoril 25 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aldoril 25, including repackagers and relabelers. The FDA regulates Aldoril 25 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aldoril 25 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 Aldoril 25 supplier is an individual or a company that provides Aldoril 25 active pharmaceutical ingredient (API) or Aldoril 25 finished formulations upon request. The Aldoril 25 suppliers may include Aldoril 25 API manufacturers, exporters, distributors and traders.
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A Aldoril 25 CEP of the European Pharmacopoeia monograph is often referred to as a Aldoril 25 Certificate of Suitability (COS). The purpose of a Aldoril 25 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aldoril 25 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aldoril 25 to their clients by showing that a Aldoril 25 CEP has been issued for it. The manufacturer submits a Aldoril 25 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aldoril 25 CEP holder for the record. Additionally, the data presented in the Aldoril 25 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aldoril 25 DMF.
A Aldoril 25 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aldoril 25 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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