01 1BCN Peptides S. A.
02 1ILS Corporation
01 1Elcatonin
02 1Salmon calcitonin "Ito"
01 1Spain
02 1U.S.A
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 : 1-2-1 Kubogaoka, Moriya City, Ibaraki Prefecture
Initial Date of Registration : 2006-09-22
Latest Date of Registration : 2009-03-26
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PharmaCompass offers a list of Calcitonin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Calcitonin manufacturer or Calcitonin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcitonin manufacturer or Calcitonin supplier.
A Elcatonin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Elcatonin, including repackagers and relabelers. The FDA regulates Elcatonin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Elcatonin 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 Elcatonin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Elcatonin supplier is an individual or a company that provides Elcatonin active pharmaceutical ingredient (API) or Elcatonin finished formulations upon request. The Elcatonin suppliers may include Elcatonin API manufacturers, exporters, distributors and traders.
click here to find a list of Elcatonin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Elcatonin Drug Master File in Japan (Elcatonin JDMF) empowers Elcatonin 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 Elcatonin JDMF during the approval evaluation for pharmaceutical products. At the time of Elcatonin 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 Elcatonin suppliers with JDMF on PharmaCompass.
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