Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem Americas, Inc.
02 1BCN Peptides S. A.
03 1ILS Inc.
01 1Elcatonin
02 1Elcatonin
03 1Salmon calcitonin "Ito"
01 1Spain
02 1Switzerland
03 1U.S.A
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 218MF10953
Registrant's Address : 3132 Kashiwa Street, Torrance, California 90505, USA
Initial Date of Registration : 2006-11-24
Latest Date of Registration : 2006-11-24
Registration Number : 223MF10073
Registrant's Address : Poligono industrial Els Vinyets-Els Fogars. Sector II 08777-Sant Quinti de Mediona, B...
Initial Date of Registration : 2011-05-27
Latest Date of Registration : 2015-08-03
Registration Number : 218MF10773
Registrant's Address : 2-1 Kubogaoka 1-chome, Moriya City, Ibaraki Prefecture
Initial Date of Registration : 2006-09-22
Latest Date of Registration : 2009-03-26
A Calcitonin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcitonin, including repackagers and relabelers. The FDA regulates Calcitonin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcitonin 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 Calcitonin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcitonin supplier is an individual or a company that provides Calcitonin active pharmaceutical ingredient (API) or Calcitonin finished formulations upon request. The Calcitonin suppliers may include Calcitonin API manufacturers, exporters, distributors and traders.
click here to find a list of Calcitonin 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 Calcitonin Drug Master File in Japan (Calcitonin JDMF) empowers Calcitonin 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 Calcitonin JDMF during the approval evaluation for pharmaceutical products. At the time of Calcitonin 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 Calcitonin suppliers with JDMF on PharmaCompass.
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