Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
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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
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01 6Adrenaline
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01 1China
02 2Germany
03 1India
04 1Luxembourg
05 1U.S.A
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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Status : Withdrawn by Holder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 Suprarenin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Suprarenin, including repackagers and relabelers. The FDA regulates Suprarenin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Suprarenin 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 Suprarenin supplier is an individual or a company that provides Suprarenin active pharmaceutical ingredient (API) or Suprarenin finished formulations upon request. The Suprarenin suppliers may include Suprarenin API manufacturers, exporters, distributors and traders.
click here to find a list of Suprarenin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Suprarenin CEP of the European Pharmacopoeia monograph is often referred to as a Suprarenin Certificate of Suitability (COS). The purpose of a Suprarenin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Suprarenin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Suprarenin to their clients by showing that a Suprarenin CEP has been issued for it. The manufacturer submits a Suprarenin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Suprarenin CEP holder for the record. Additionally, the data presented in the Suprarenin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Suprarenin DMF.
A Suprarenin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Suprarenin 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 Suprarenin suppliers with CEP (COS) on PharmaCompass.
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