01 1Curia Spain S. A. U.
01 1Ulipristal acetate micronized
01 1U.S.A
Registration Number : 301MF10081
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2019-10-25
Latest Date of Registration : 2019-10-25
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PharmaCompass offers a list of Ulipristal 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 Ulipristal Acetate manufacturer or Ulipristal Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ulipristal Acetate manufacturer or Ulipristal Acetate supplier.
PharmaCompass also assists you with knowing the Ulipristal Acetate API Price utilized in the formulation of products. Ulipristal Acetate API Price is not always fixed or binding as the Ulipristal Acetate Price is obtained through a variety of data sources. The Ulipristal Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ulipristal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ulipristal, including repackagers and relabelers. The FDA regulates Ulipristal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ulipristal 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 Ulipristal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ulipristal supplier is an individual or a company that provides Ulipristal active pharmaceutical ingredient (API) or Ulipristal finished formulations upon request. The Ulipristal suppliers may include Ulipristal API manufacturers, exporters, distributors and traders.
click here to find a list of Ulipristal 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 Ulipristal Drug Master File in Japan (Ulipristal JDMF) empowers Ulipristal 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 Ulipristal JDMF during the approval evaluation for pharmaceutical products. At the time of Ulipristal 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 Ulipristal suppliers with JDMF on PharmaCompass.
