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
A Glucagon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucagon, including repackagers and relabelers. The FDA regulates Glucagon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucagon 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 Glucagon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glucagon supplier is an individual or a company that provides Glucagon active pharmaceutical ingredient (API) or Glucagon finished formulations upon request. The Glucagon suppliers may include Glucagon API manufacturers, exporters, distributors and traders.
click here to find a list of Glucagon 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 Glucagon Drug Master File in Japan (Glucagon JDMF) empowers Glucagon 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 Glucagon JDMF during the approval evaluation for pharmaceutical products. At the time of Glucagon 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 Glucagon suppliers with JDMF on PharmaCompass.
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