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.
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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 LOGILIA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LOGILIA, including repackagers and relabelers. The FDA regulates LOGILIA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LOGILIA 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 LOGILIA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LOGILIA supplier is an individual or a company that provides LOGILIA active pharmaceutical ingredient (API) or LOGILIA finished formulations upon request. The LOGILIA suppliers may include LOGILIA API manufacturers, exporters, distributors and traders.
click here to find a list of LOGILIA 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 LOGILIA Drug Master File in Japan (LOGILIA JDMF) empowers LOGILIA 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 LOGILIA JDMF during the approval evaluation for pharmaceutical products. At the time of LOGILIA 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 LOGILIA suppliers with JDMF on PharmaCompass.
