Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG
01 1Squid ibant acetate
01 1Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 229MF10071
Registrant's Address : Hauptstrasse 144,4416 Bubendorf Switzerland
Initial Date of Registration : 2017-04-04
Latest Date of Registration : 2018-09-03
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PharmaCompass offers a list of Icatibant 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 Icatibant Acetate manufacturer or Icatibant Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Icatibant Acetate API Price utilized in the formulation of products. Icatibant Acetate API Price is not always fixed or binding as the Icatibant Acetate Price is obtained through a variety of data sources. The Icatibant Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Icatibant Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Icatibant Acetate, including repackagers and relabelers. The FDA regulates Icatibant Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Icatibant 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.
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A Icatibant Acetate supplier is an individual or a company that provides Icatibant Acetate active pharmaceutical ingredient (API) or Icatibant Acetate finished formulations upon request. The Icatibant Acetate suppliers may include Icatibant Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Icatibant Acetate 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 Icatibant Acetate Drug Master File in Japan (Icatibant Acetate JDMF) empowers Icatibant Acetate 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 Icatibant Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Icatibant Acetate 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 Icatibant Acetate suppliers with JDMF on PharmaCompass.
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