01 1Curia Spain S. A. U.
01 1Mifepristone micronized
01 1U.S.A
Registration Number : 302MF10146
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2020-12-15
Latest Date of Registration : 2020-12-15
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PharmaCompass offers a list of Mifepristone 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 Mifepristone manufacturer or Mifepristone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mifepristone manufacturer or Mifepristone supplier.
PharmaCompass also assists you with knowing the Mifepristone API Price utilized in the formulation of products. Mifepristone API Price is not always fixed or binding as the Mifepristone Price is obtained through a variety of data sources. The Mifepristone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VGX-410 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VGX-410, including repackagers and relabelers. The FDA regulates VGX-410 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VGX-410 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 VGX-410 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A VGX-410 supplier is an individual or a company that provides VGX-410 active pharmaceutical ingredient (API) or VGX-410 finished formulations upon request. The VGX-410 suppliers may include VGX-410 API manufacturers, exporters, distributors and traders.
click here to find a list of VGX-410 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 VGX-410 Drug Master File in Japan (VGX-410 JDMF) empowers VGX-410 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 VGX-410 JDMF during the approval evaluation for pharmaceutical products. At the time of VGX-410 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 VGX-410 suppliers with JDMF on PharmaCompass.
