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
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PharmaCompass offers a list of Alclometasone Dipropionate 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 Alclometasone Dipropionate manufacturer or Alclometasone Dipropionate supplier for your needs.
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PharmaCompass also assists you with knowing the Alclometasone Dipropionate API Price utilized in the formulation of products. Alclometasone Dipropionate API Price is not always fixed or binding as the Alclometasone Dipropionate Price is obtained through a variety of data sources. The Alclometasone Dipropionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alclometasone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alclometasone, including repackagers and relabelers. The FDA regulates Alclometasone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alclometasone 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 Alclometasone supplier is an individual or a company that provides Alclometasone active pharmaceutical ingredient (API) or Alclometasone finished formulations upon request. The Alclometasone suppliers may include Alclometasone API manufacturers, exporters, distributors and traders.
click here to find a list of Alclometasone 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 Drug Master File in Japan (Alclometasone JDMF) empowers Alclometasone 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Alclometasone 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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