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01 1EUROAPI GERMANY GmbH Frankfurt am Main DE
02 1ASPEN OSS B.V. Oss NL
03 1Bachem AG Bubendorf CH
01 3Gonadorelin acetate
01 1France
02 1Netherlands
03 1Switzerland
01 3Valid
Certificate Number : R1-CEP 1997-110 - Rev 02
Status : Valid
Issue Date : 2021-12-09
Type : Chemical
Substance Number : 827
Certificate Number : R1-CEP 2011-073 - Rev 01
Status : Valid
Issue Date : 2018-07-23
Type : Chemical
Substance Number : 827
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 2005-022 - Rev 01
Status : Valid
Issue Date : 2018-06-14
Type : Chemical
Substance Number : 827
A Gonadorelin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gonadorelin Acetate, including repackagers and relabelers. The FDA regulates Gonadorelin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gonadorelin Acetate 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 Gonadorelin Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gonadorelin Acetate supplier is an individual or a company that provides Gonadorelin Acetate active pharmaceutical ingredient (API) or Gonadorelin Acetate finished formulations upon request. The Gonadorelin Acetate suppliers may include Gonadorelin Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Gonadorelin Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gonadorelin Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Gonadorelin Acetate Certificate of Suitability (COS). The purpose of a Gonadorelin Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Gonadorelin Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Gonadorelin Acetate to their clients by showing that a Gonadorelin Acetate CEP has been issued for it. The manufacturer submits a Gonadorelin Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Gonadorelin Acetate CEP holder for the record. Additionally, the data presented in the Gonadorelin Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Gonadorelin Acetate DMF.
A Gonadorelin Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Gonadorelin Acetate 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 Gonadorelin Acetate suppliers with CEP (COS) on PharmaCompass.
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