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
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.
click here to find a list of Icatibant Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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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