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 2U.S.A
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 : CEP 2015-006 - Rev 02
Status : Valid
Issue Date : 2025-09-24
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
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A nchembio747-comp9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of nchembio747-comp9, including repackagers and relabelers. The FDA regulates nchembio747-comp9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. nchembio747-comp9 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 nchembio747-comp9 supplier is an individual or a company that provides nchembio747-comp9 active pharmaceutical ingredient (API) or nchembio747-comp9 finished formulations upon request. The nchembio747-comp9 suppliers may include nchembio747-comp9 API manufacturers, exporters, distributors and traders.
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A nchembio747-comp9 CEP of the European Pharmacopoeia monograph is often referred to as a nchembio747-comp9 Certificate of Suitability (COS). The purpose of a nchembio747-comp9 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of nchembio747-comp9 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of nchembio747-comp9 to their clients by showing that a nchembio747-comp9 CEP has been issued for it. The manufacturer submits a nchembio747-comp9 CEP (COS) as part of the market authorization procedure, and it takes on the role of a nchembio747-comp9 CEP holder for the record. Additionally, the data presented in the nchembio747-comp9 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the nchembio747-comp9 DMF.
A nchembio747-comp9 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. nchembio747-comp9 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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