Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 2BACHEM S.A. Vionnaz CH
02 1HUZHOU ZHANWANG PHARMACEUTICAL CO., LTD. Linghu Town CN
03 1JANSSEN PHARMACEUTICA NV Beerse BE
04 1PISGAH LABORATORIES INC. Pisgah Forest US
05 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
01 5Etomidate
02 1Etomidate, Process B
01 1Belgium
02 1China
03 1India
04 2Switzerland
05 1U.S.A
01 5Valid
02 1Withdrawn by Holder
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Certificate Number : R0-CEP 2020-417 - Rev 00
Status : Valid
Issue Date : 2022-05-06
Type : Chemical
Substance Number : 1514
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Certificate Number : CEP 2005-250 - Rev 03
Status : Valid
Issue Date : 2024-03-20
Type : Chemical
Substance Number : 1514
Certificate Number : R1-CEP 2016-298 - Rev 00
Status : Valid
Issue Date : 2023-04-21
Type : Chemical
Substance Number : 1514
Certificate Number : R1-CEP 2002-080 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2017-11-03
Type : Chemical
Substance Number : 1514
Certificate Number : R0-CEP 2020-231 - Rev 01
Status : Valid
Issue Date : 2022-05-10
Type : Chemical
Substance Number : 1514
Certificate Number : CEP 2017-278 - Rev 02
Status : Valid
Issue Date : 2024-09-27
Type : Chemical
Substance Number : 1514
A Etomidate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etomidate, including repackagers and relabelers. The FDA regulates Etomidate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etomidate 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 Etomidate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etomidate supplier is an individual or a company that provides Etomidate active pharmaceutical ingredient (API) or Etomidate finished formulations upon request. The Etomidate suppliers may include Etomidate API manufacturers, exporters, distributors and traders.
click here to find a list of Etomidate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etomidate CEP of the European Pharmacopoeia monograph is often referred to as a Etomidate Certificate of Suitability (COS). The purpose of a Etomidate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etomidate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etomidate to their clients by showing that a Etomidate CEP has been issued for it. The manufacturer submits a Etomidate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etomidate CEP holder for the record. Additionally, the data presented in the Etomidate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etomidate DMF.
A Etomidate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etomidate 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 Etomidate suppliers with CEP (COS) on PharmaCompass.
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