Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1TRANSO-PHARM HANDELS GMBH Siek DE
02 1CAMBREX PROFARMACO MILANO S.R.L. Paullo IT
03 1MATRIX PHARMACORP PRIVATE LIMITED Sangareddy District IN
04 1WUHAN WUYAO PHARMACEUTICAL CO., LTD. Huangshi City CN
01 4Adrenaline
01 1China
02 1Germany
03 1U.S.A
04 1Blank
01 4Valid
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Certificate Number : R1-CEP 2016-232 - Rev 00
Status : Valid
Issue Date : 2023-02-09
Type : Chemical
Substance Number : 2303
Certificate Number : R1-CEP 2013-266 - Rev 01
Status : Valid
Issue Date : 2023-01-31
Type : Chemical
Substance Number : 2303
Certificate Number : R0-CEP 2020-192 - Rev 02
Status : Valid
Issue Date : 2023-02-16
Type : Chemical
Substance Number : 2303
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
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Corporate PDF
Certificate Number : CEP 2015-006 - Rev 02
Status : Valid
Issue Date : 2025-09-24
Type : Chemical
Substance Number : 2303
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Epinephrine 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 Epinephrine manufacturer or Epinephrine supplier for your needs.
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A Auvi-q manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Auvi-q, including repackagers and relabelers. The FDA regulates Auvi-q manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Auvi-q 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 Auvi-q supplier is an individual or a company that provides Auvi-q active pharmaceutical ingredient (API) or Auvi-q finished formulations upon request. The Auvi-q suppliers may include Auvi-q API manufacturers, exporters, distributors and traders.
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A Auvi-q CEP of the European Pharmacopoeia monograph is often referred to as a Auvi-q Certificate of Suitability (COS). The purpose of a Auvi-q CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Auvi-q EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Auvi-q to their clients by showing that a Auvi-q CEP has been issued for it. The manufacturer submits a Auvi-q CEP (COS) as part of the market authorization procedure, and it takes on the role of a Auvi-q CEP holder for the record. Additionally, the data presented in the Auvi-q CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Auvi-q DMF.
A Auvi-q CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Auvi-q 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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