Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
01 1Curia Spain S. A. U.
01 1Prednisolone Sodium Phosphate
01 1U.S.A
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Registration Number : 217MF10681
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2010-04-05
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PharmaCompass offers a list of Prednisolone Sodium Phosphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Prednisolone Sodium Phosphate manufacturer or Prednisolone Sodium Phosphate supplier for your needs.
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A Metreton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metreton, including repackagers and relabelers. The FDA regulates Metreton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metreton 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 Metreton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Metreton supplier is an individual or a company that provides Metreton active pharmaceutical ingredient (API) or Metreton finished formulations upon request. The Metreton suppliers may include Metreton API manufacturers, exporters, distributors and traders.
click here to find a list of Metreton suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Metreton Drug Master File in Japan (Metreton JDMF) empowers Metreton 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 Metreton JDMF during the approval evaluation for pharmaceutical products. At the time of Metreton 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 Metreton suppliers with JDMF on PharmaCompass.
