Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG Bubendorf CH
02 1BCN PEPTIDES S.A. St Quinti De Mediona ES
03 1CHEMI S.P.A. Patrica IT
04 1N.V. ORGANON Oss NL
01 4Goserelin
01 1Italy
02 1Spain
03 1Switzerland
04 1U.S.A
01 2Valid
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 : R1-CEP 2003-037 - Rev 03
Status : Valid
Issue Date : 2020-12-18
Type : Chemical
Substance Number : 1636
Certificate Number : R1-CEP 2007-183 - Rev 01
Status : Valid
Issue Date : 2014-06-12
Type : Chemical
Substance Number : 1636
Certificate Number : R1-CEP 2005-276 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2017-01-31
Type : Chemical
Substance Number : 1636
Certificate Number : R0-CEP 2009-123 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2010-07-22
Type : Chemical
Substance Number : 1636
A Goserelin acetate (JAN/USP) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Goserelin acetate (JAN/USP), including repackagers and relabelers. The FDA regulates Goserelin acetate (JAN/USP) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Goserelin acetate (JAN/USP) 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 Goserelin acetate (JAN/USP) supplier is an individual or a company that provides Goserelin acetate (JAN/USP) active pharmaceutical ingredient (API) or Goserelin acetate (JAN/USP) finished formulations upon request. The Goserelin acetate (JAN/USP) suppliers may include Goserelin acetate (JAN/USP) API manufacturers, exporters, distributors and traders.
click here to find a list of Goserelin acetate (JAN/USP) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Goserelin acetate (JAN/USP) CEP of the European Pharmacopoeia monograph is often referred to as a Goserelin acetate (JAN/USP) Certificate of Suitability (COS). The purpose of a Goserelin acetate (JAN/USP) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Goserelin acetate (JAN/USP) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Goserelin acetate (JAN/USP) to their clients by showing that a Goserelin acetate (JAN/USP) CEP has been issued for it. The manufacturer submits a Goserelin acetate (JAN/USP) CEP (COS) as part of the market authorization procedure, and it takes on the role of a Goserelin acetate (JAN/USP) CEP holder for the record. Additionally, the data presented in the Goserelin acetate (JAN/USP) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Goserelin acetate (JAN/USP) DMF.
A Goserelin acetate (JAN/USP) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Goserelin acetate (JAN/USP) 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 Goserelin acetate (JAN/USP) suppliers with CEP (COS) on PharmaCompass.
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