Aspen API. More than just an API™
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01 1ASPEN OSS B.V. Oss NL
02 1Bachem AG Bubendorf CH
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01 2Gonadorelin acetate
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01 1Netherlands
02 1Switzerland
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01 2Valid
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
95
PharmaCompass offers a list of Gonadorelin Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Gonadorelin Acetate manufacturer or Gonadorelin Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gonadorelin Acetate manufacturer or Gonadorelin Acetate supplier.
PharmaCompass also assists you with knowing the Gonadorelin Acetate API Price utilized in the formulation of products. Gonadorelin Acetate API Price is not always fixed or binding as the Gonadorelin Acetate Price is obtained through a variety of data sources. The Gonadorelin Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutrelef manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutrelef, including repackagers and relabelers. The FDA regulates Lutrelef manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutrelef 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 Lutrelef manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lutrelef supplier is an individual or a company that provides Lutrelef active pharmaceutical ingredient (API) or Lutrelef finished formulations upon request. The Lutrelef suppliers may include Lutrelef API manufacturers, exporters, distributors and traders.
click here to find a list of Lutrelef suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lutrelef CEP of the European Pharmacopoeia monograph is often referred to as a Lutrelef Certificate of Suitability (COS). The purpose of a Lutrelef CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lutrelef EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lutrelef to their clients by showing that a Lutrelef CEP has been issued for it. The manufacturer submits a Lutrelef CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lutrelef CEP holder for the record. Additionally, the data presented in the Lutrelef CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lutrelef DMF.
A Lutrelef CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lutrelef 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 Lutrelef suppliers with CEP (COS) on PharmaCompass.