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 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
03 1Cambrex Profarmaco Milano S.r.l. Paullo IT
04 1ROUVER INVESTMENT S.A.R.L. Luxembourg LU
05 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
06 1WUHAN WUYAO PHARMACEUTICAL CO., LTD. Huangshi City CN
01 6Adrenaline
01 1China
02 2Germany
03 1India
04 1Luxembourg
05 1U.S.A
01 1Expired
02 4Valid
03 1Withdrawn by Holder
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 2009-274 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2016-03-17
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 : CEP 2015-006 - Rev 01
Status : Valid
Issue Date : 2024-07-29
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
Certificate Number : R0-CEP 2014-043 - Rev 00
Status : Expired
Issue Date : 2015-03-13
Type : Chemical
Substance Number : 2303
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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 Vasoton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vasoton, including repackagers and relabelers. The FDA regulates Vasoton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vasoton API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Vasoton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vasoton supplier is an individual or a company that provides Vasoton active pharmaceutical ingredient (API) or Vasoton finished formulations upon request. The Vasoton suppliers may include Vasoton API manufacturers, exporters, distributors and traders.
click here to find a list of Vasoton suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vasoton CEP of the European Pharmacopoeia monograph is often referred to as a Vasoton Certificate of Suitability (COS). The purpose of a Vasoton CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vasoton EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vasoton to their clients by showing that a Vasoton CEP has been issued for it. The manufacturer submits a Vasoton CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vasoton CEP holder for the record. Additionally, the data presented in the Vasoton CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vasoton DMF.
A Vasoton CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vasoton CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Vasoton suppliers with CEP (COS) on PharmaCompass.
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