Axplora is your partner of choice for complex APIs.
01 1Farmabios S. p. A.
01 1Medroxyprogesterone acetate
01 1Germany
Axplora is your 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
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PharmaCompass offers a list of Medroxyprogesterone Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Medroxyprogesterone Acetate manufacturer or Medroxyprogesterone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Medroxyprogesterone Acetate manufacturer or Medroxyprogesterone Acetate supplier.
PharmaCompass also assists you with knowing the Medroxyprogesterone Acetate API Price utilized in the formulation of products. Medroxyprogesterone Acetate API Price is not always fixed or binding as the Medroxyprogesterone Acetate Price is obtained through a variety of data sources. The Medroxyprogesterone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MPA-beta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MPA-beta, including repackagers and relabelers. The FDA regulates MPA-beta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MPA-beta 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 MPA-beta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MPA-beta supplier is an individual or a company that provides MPA-beta active pharmaceutical ingredient (API) or MPA-beta finished formulations upon request. The MPA-beta suppliers may include MPA-beta API manufacturers, exporters, distributors and traders.
click here to find a list of MPA-beta 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 MPA-beta Drug Master File in Japan (MPA-beta JDMF) empowers MPA-beta 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 MPA-beta JDMF during the approval evaluation for pharmaceutical products. At the time of MPA-beta 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 MPA-beta suppliers with JDMF on PharmaCompass.
