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Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides. 
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01 Bachem AG (1)
01 Goserelin Acetate (1)
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PharmaCompass offers a list of Goserelin 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 Goserelin Acetate manufacturer or Goserelin Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Goserelin Acetate manufacturer or Goserelin Acetate supplier.
PharmaCompass also assists you with knowing the Goserelin Acetate API Price utilized in the formulation of products. Goserelin Acetate API Price is not always fixed or binding as the Goserelin Acetate Price is obtained through a variety of data sources. The Goserelin Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Goserelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Goserelin, including repackagers and relabelers. The FDA regulates Goserelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Goserelin 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 Goserelin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Goserelin supplier is an individual or a company that provides Goserelin active pharmaceutical ingredient (API) or Goserelin finished formulations upon request. The Goserelin suppliers may include Goserelin API manufacturers, exporters, distributors and traders.
click here to find a list of Goserelin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Goserelin Drug Master File in Japan (Goserelin JDMF) empowers Goserelin API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Goserelin JDMF during the approval evaluation for pharmaceutical products. At the time of Goserelin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Goserelin suppliers with JDMF on PharmaCompass.
