Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1COHANCE LIFESCIENCES LIMITED Hyderabad IN
02 2CHEMISCHE FABRIK BERG GMBH Bitterfeld-Wolfen DE
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1EXCELLA GMBH & CO. KG Feucht DE
05 2MIDAS PHARMA GMBH Ingelheim am Rhein DE
06 1NIFTY LABS PRIVATE LIMITED Hyderabad IN
07 1NOSCH LABS PRIVATE LIMITED Hyderabad IN
08 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2010-312 - Rev 03
Status : Valid
Issue Date : 2023-10-27
Type : Chemical
Substance Number : 2125
Certificate Number : CEP 2022-316 - Rev 00
Status : Valid
Issue Date : 2024-04-29
Type : Chemical
Substance Number : 2125
Certificate Number : CEP 2024-489 - Rev 00
Status : Valid
Issue Date : 2025-01-27
Type : Chemical
Substance Number : 2125
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PharmaCompass offers a list of Doxazosin Mesylate 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 Doxazosin Mesylate manufacturer or Doxazosin Mesylate supplier for your needs.
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A Diblocin Uro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diblocin Uro, including repackagers and relabelers. The FDA regulates Diblocin Uro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diblocin Uro 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 Diblocin Uro supplier is an individual or a company that provides Diblocin Uro active pharmaceutical ingredient (API) or Diblocin Uro finished formulations upon request. The Diblocin Uro suppliers may include Diblocin Uro API manufacturers, exporters, distributors and traders.
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A Diblocin Uro CEP of the European Pharmacopoeia monograph is often referred to as a Diblocin Uro Certificate of Suitability (COS). The purpose of a Diblocin Uro CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Diblocin Uro EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Diblocin Uro to their clients by showing that a Diblocin Uro CEP has been issued for it. The manufacturer submits a Diblocin Uro CEP (COS) as part of the market authorization procedure, and it takes on the role of a Diblocin Uro CEP holder for the record. Additionally, the data presented in the Diblocin Uro CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Diblocin Uro DMF.
A Diblocin Uro CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Diblocin Uro 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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