Axplora- The partner of choice for complex APIs.
01 1Farmabios S. p. A.
01 1Medroxyprogesterone acetate
01 1Germany
Axplora- The partner of choice for complex APIs.
Registration Number : 222MF10098
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2010-03-17
Latest Date of Registration : 2019-05-27
A Medroxyprogesterone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Medroxyprogesterone Acetate, including repackagers and relabelers. The FDA regulates Medroxyprogesterone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Medroxyprogesterone 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 Medroxyprogesterone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Medroxyprogesterone Acetate supplier is an individual or a company that provides Medroxyprogesterone Acetate active pharmaceutical ingredient (API) or Medroxyprogesterone Acetate finished formulations upon request. The Medroxyprogesterone Acetate suppliers may include Medroxyprogesterone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Medroxyprogesterone 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 Medroxyprogesterone Acetate Drug Master File in Japan (Medroxyprogesterone Acetate JDMF) empowers Medroxyprogesterone 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 Medroxyprogesterone Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Medroxyprogesterone 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 Medroxyprogesterone Acetate suppliers with JDMF on PharmaCompass.
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