Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1BACHEM SA Vionnaz CH
02 2EMCURE PHARMACEUTICALS LIMITED Pune IN
03 1F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
04 1GUANGDONG JIABO PHARMACEUTICAL CO., LTD. Qingyuan CN
05 1HARMAN FINOCHEM LIMITED Mumbai IN
06 1MIDAS PHARMA GMBH Ingelheim am Rhein DE
07 1SI GROUP, INC. The Woodlands US
08 1Themis Medicare Ltd. Vapi IN
01 7Propofol
02 1Propofol, Code number 4037808
03 1Propofol, PFL
01 1China
02 1Germany
03 4India
04 1Italy
05 1Switzerland
06 1U.S.A
01 7Valid
02 2Withdrawn 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 : CEP 2005-003 - Rev 05
Status : Valid
Issue Date : 2024-09-04
Type : Chemical
Substance Number : 1558
Certificate Number : CEP 2020-203 - Rev 02
Status : Valid
Issue Date : 2025-12-01
Type : Chemical
Substance Number : 1558
Certificate Number : CEP 2024-066 - Rev 00
Status : Valid
Issue Date : 2024-07-12
Type : Chemical
Substance Number : 1558
Certificate Number : R1-CEP 2004-313 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2017-03-01
Type : Chemical
Substance Number : 1558
Certificate Number : R0-CEP 2022-494 - Rev 00
Status : Valid
Issue Date : 2023-08-07
Type : Chemical
Substance Number : 1558
Certificate Number : CEP 2015-347 - Rev 02
Status : Valid
Issue Date : 2025-04-02
Type : Chemical
Substance Number : 1558
Certificate Number : R0-CEP 2021-363 - Rev 00
Status : Valid
Issue Date : 2022-02-08
Type : Chemical
Substance Number : 1558
Certificate Number : CEP 2002-229 - Rev 05
Status : Valid
Issue Date : 2025-05-30
Type : Chemical
Substance Number : 1558
Certificate Number : R0-CEP 2004-218 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2005-10-13
Type : Chemical
Substance Number : 1558
37
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A Disoprivan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disoprivan, including repackagers and relabelers. The FDA regulates Disoprivan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disoprivan 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 Disoprivan supplier is an individual or a company that provides Disoprivan active pharmaceutical ingredient (API) or Disoprivan finished formulations upon request. The Disoprivan suppliers may include Disoprivan API manufacturers, exporters, distributors and traders.
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A Disoprivan CEP of the European Pharmacopoeia monograph is often referred to as a Disoprivan Certificate of Suitability (COS). The purpose of a Disoprivan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Disoprivan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Disoprivan to their clients by showing that a Disoprivan CEP has been issued for it. The manufacturer submits a Disoprivan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Disoprivan CEP holder for the record. Additionally, the data presented in the Disoprivan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Disoprivan DMF.
A Disoprivan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Disoprivan 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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