Axplora is your partner of choice for complex APIs.
01 1Farmabios S. p. A.
02 1Pfizer Inc.
03 1Sogo Pharmaceutical Co., Ltd.
01 2Chlormadinone Acetate
02 1Japanese Pharmacopoeia chlormadinone acetate ester
01 1Germany
02 1Japan
03 1U.S.A
Axplora is your partner of choice for complex APIs.
Registration Number : 218MF10991
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2019-07-04
Japanese Pharmacopoeia Chlormadinone Acetate
Registration Number : 218MF10701
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
Registration Number : 217MF10977
Registrant's Address : 235 East 42nd Street, New York, NY 10017
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2009-05-27
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PharmaCompass offers a list of Chlormadinone Acetate 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 Chlormadinone Acetate manufacturer or Chlormadinone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlormadinone Acetate manufacturer or Chlormadinone Acetate supplier.
A Gestafortin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gestafortin, including repackagers and relabelers. The FDA regulates Gestafortin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gestafortin 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 Gestafortin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Gestafortin supplier is an individual or a company that provides Gestafortin active pharmaceutical ingredient (API) or Gestafortin finished formulations upon request. The Gestafortin suppliers may include Gestafortin API manufacturers, exporters, distributors and traders.
click here to find a list of Gestafortin 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 Gestafortin Drug Master File in Japan (Gestafortin JDMF) empowers Gestafortin 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 Gestafortin JDMF during the approval evaluation for pharmaceutical products. At the time of Gestafortin 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 Gestafortin suppliers with JDMF on PharmaCompass.
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