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.
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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 ZK 98296 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZK 98296, including repackagers and relabelers. The FDA regulates ZK 98296 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZK 98296 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ZK 98296 supplier is an individual or a company that provides ZK 98296 active pharmaceutical ingredient (API) or ZK 98296 finished formulations upon request. The ZK 98296 suppliers may include ZK 98296 API manufacturers, exporters, distributors and traders.
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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 ZK 98296 Drug Master File in Japan (ZK 98296 JDMF) empowers ZK 98296 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 ZK 98296 JDMF during the approval evaluation for pharmaceutical products. At the time of ZK 98296 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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