01 1Active Pharma Inc.
01 1Outsiders regulations flutazolam (production only)
01 1Japan
Flutazolam (for manufacturing only)
Registration Number : 217MF10196
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-08
Latest Date of Registration : 2009-09-14
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PharmaCompass offers a list of Flutazolam 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 Flutazolam manufacturer or Flutazolam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flutazolam manufacturer or Flutazolam supplier.
PharmaCompass also assists you with knowing the Flutazolam API Price utilized in the formulation of products. Flutazolam API Price is not always fixed or binding as the Flutazolam Price is obtained through a variety of data sources. The Flutazolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flutazolam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flutazolam, including repackagers and relabelers. The FDA regulates Flutazolam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flutazolam API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Flutazolam supplier is an individual or a company that provides Flutazolam active pharmaceutical ingredient (API) or Flutazolam finished formulations upon request. The Flutazolam suppliers may include Flutazolam API manufacturers, exporters, distributors and traders.
click here to find a list of Flutazolam 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 Flutazolam Drug Master File in Japan (Flutazolam JDMF) empowers Flutazolam 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 Flutazolam JDMF during the approval evaluation for pharmaceutical products. At the time of Flutazolam 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 Flutazolam suppliers with JDMF on PharmaCompass.
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