Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1ZHEJIANG HENGKANG PHARMACEUTICAL CO., LTD. Sanmen CN
02 1SIEGFRIED AG Zofingen CH
03 1SIEGFRIED LTD. Zofingen CH
01 1Acemetacin, Code 100033
02 1Acemetacin, Polymorphic form II
03 1Acemetacin, Pubagang site
01 1China
02 2Switzerland
01 3Valid
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Certificate Number : R0-CEP 2022-226 - Rev 00
Status : Valid
Issue Date : 2022-11-10
Type : Chemical
Substance Number : 1686
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Certificate Number : R1-CEP 2012-211 - Rev 02
Status : Valid
Issue Date : 2021-04-19
Type : Chemical
Substance Number : 1686
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
Acemetacin, Polymorphic Form II
Certificate Number : CEP 2018-306 - Rev 01
Status : Valid
Issue Date : 2024-06-25
Type : Chemical
Substance Number : 1686
74
PharmaCompass offers a list of Acemetacin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Acemetacin manufacturer or Acemetacin supplier for your needs.
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A Acemetacin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acemetacin, including repackagers and relabelers. The FDA regulates Acemetacin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acemetacin 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 Acemetacin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Acemetacin supplier is an individual or a company that provides Acemetacin active pharmaceutical ingredient (API) or Acemetacin finished formulations upon request. The Acemetacin suppliers may include Acemetacin API manufacturers, exporters, distributors and traders.
click here to find a list of Acemetacin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Acemetacin CEP of the European Pharmacopoeia monograph is often referred to as a Acemetacin Certificate of Suitability (COS). The purpose of a Acemetacin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Acemetacin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Acemetacin to their clients by showing that a Acemetacin CEP has been issued for it. The manufacturer submits a Acemetacin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Acemetacin CEP holder for the record. Additionally, the data presented in the Acemetacin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Acemetacin DMF.
A Acemetacin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Acemetacin 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 Acemetacin suppliers with CEP (COS) on PharmaCompass.
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