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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A Glucagon, pig manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucagon, pig, including repackagers and relabelers. The FDA regulates Glucagon, pig manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucagon, pig 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 Glucagon, pig supplier is an individual or a company that provides Glucagon, pig active pharmaceutical ingredient (API) or Glucagon, pig finished formulations upon request. The Glucagon, pig suppliers may include Glucagon, pig 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 Glucagon, pig Drug Master File in Japan (Glucagon, pig JDMF) empowers Glucagon, pig 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, pig JDMF during the approval evaluation for pharmaceutical products. At the time of Glucagon, pig 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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