Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG
02 1BCN Peptides S. A.
03 1ILS Inc.
04 1Peptisyntha, Inc.
01 2Buserelin
02 1Buserelin acetate "Ito"
03 1Buserelin acetate "Mitsuba"
01 1Germany
02 1Spain
03 1Switzerland
04 1U.S.A
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 225MF10159
Registrant's Address : Hauptstrasse 144,4416 Bubendorf Switzerland
Initial Date of Registration : 2013-08-14
Latest Date of Registration : 2013-08-14
Registration Number : 305MF10126
Registrant's Address : Poligono industrial Els Vinyets-Els Fogars. Sector II 08777-Sant Quinti de Mediona, B...
Initial Date of Registration : 2023-11-29
Latest Date of Registration : 2023-11-29
Registration Number : 219MF10206
Registrant's Address : 20910 Higgins Court Torrance, California USA 90501-1722
Initial Date of Registration : 2007-06-13
Latest Date of Registration : 2007-06-13
Registration Number : 219MF10292
Registrant's Address : Randic Kanda Building, 2-6 Kanda Sudacho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2007-09-10
Latest Date of Registration : 2007-09-10
A Buserelin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buserelin Acetate, including repackagers and relabelers. The FDA regulates Buserelin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buserelin 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 Buserelin Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Buserelin Acetate supplier is an individual or a company that provides Buserelin Acetate active pharmaceutical ingredient (API) or Buserelin Acetate finished formulations upon request. The Buserelin Acetate suppliers may include Buserelin Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Buserelin 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 Buserelin Acetate Drug Master File in Japan (Buserelin Acetate JDMF) empowers Buserelin 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 Buserelin Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Buserelin 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 Buserelin Acetate suppliers with JDMF on PharmaCompass.
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