Axplora- The 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- The 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
A Chlormadinone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlormadinone Acetate, including repackagers and relabelers. The FDA regulates Chlormadinone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlormadinone 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 Chlormadinone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlormadinone Acetate supplier is an individual or a company that provides Chlormadinone Acetate active pharmaceutical ingredient (API) or Chlormadinone Acetate finished formulations upon request. The Chlormadinone Acetate suppliers may include Chlormadinone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Chlormadinone 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 Chlormadinone Acetate Drug Master File in Japan (Chlormadinone Acetate JDMF) empowers Chlormadinone 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 Chlormadinone Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Chlormadinone 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 Chlormadinone Acetate suppliers with JDMF on PharmaCompass.
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