Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 2Bachem AG
02 1Peptisyntha, Inc.
01 1Glucagon
02 1Glucagon "Ito"
03 1Glucagon -MT
01 1Germany
02 2Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 231MF10022
Registrant's Address : Hauptstrasse 144,4416 Bubendorf Switzerland
Initial Date of Registration : 2019-01-29
Latest Date of Registration : 2019-01-29
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 218MF10708
Registrant's Address : Hauptstrasse 144,4416 Bubendorf Switzerland
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
Registration Number : 218MF10886
Registrant's Address : 20910, Higgins Court Torrance, California USA, 90501-1722
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
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PharmaCompass offers a list of Glucagon 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 Glucagon manufacturer or Glucagon supplier for your needs.
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A Glucagone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucagone, including repackagers and relabelers. The FDA regulates Glucagone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucagone 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 Glucagone supplier is an individual or a company that provides Glucagone active pharmaceutical ingredient (API) or Glucagone finished formulations upon request. The Glucagone suppliers may include Glucagone API manufacturers, exporters, distributors and traders.
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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 Glucagone Drug Master File in Japan (Glucagone JDMF) empowers Glucagone 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 Glucagone JDMF during the approval evaluation for pharmaceutical products. At the time of Glucagone JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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