01 1Curia Spain S. A. U.
01 1Propionic acid alclometasone
01 1U.S.A
Registration Number : 218MF10892
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
A Alclometasone Dipropionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alclometasone Dipropionate, including repackagers and relabelers. The FDA regulates Alclometasone Dipropionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alclometasone Dipropionate 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 Alclometasone Dipropionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alclometasone Dipropionate supplier is an individual or a company that provides Alclometasone Dipropionate active pharmaceutical ingredient (API) or Alclometasone Dipropionate finished formulations upon request. The Alclometasone Dipropionate suppliers may include Alclometasone Dipropionate API manufacturers, exporters, distributors and traders.
click here to find a list of Alclometasone Dipropionate 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 Alclometasone Dipropionate Drug Master File in Japan (Alclometasone Dipropionate JDMF) empowers Alclometasone Dipropionate 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 Alclometasone Dipropionate JDMF during the approval evaluation for pharmaceutical products. At the time of Alclometasone Dipropionate 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 Alclometasone Dipropionate suppliers with JDMF on PharmaCompass.
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