01 1Active Pharma Inc.
01 1Rilmazafone hydrochloride
01 1Japan
Registration Number : 218MF10795
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-10-06
Latest Date of Registration : 2006-10-06
A Rilmazafone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rilmazafone Hydrochloride, including repackagers and relabelers. The FDA regulates Rilmazafone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rilmazafone Hydrochloride 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 Rilmazafone Hydrochloride supplier is an individual or a company that provides Rilmazafone Hydrochloride active pharmaceutical ingredient (API) or Rilmazafone Hydrochloride finished formulations upon request. The Rilmazafone Hydrochloride suppliers may include Rilmazafone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Rilmazafone Hydrochloride 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 Rilmazafone Hydrochloride Drug Master File in Japan (Rilmazafone Hydrochloride JDMF) empowers Rilmazafone Hydrochloride 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 Rilmazafone Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Rilmazafone Hydrochloride 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 Rilmazafone Hydrochloride suppliers with JDMF on PharmaCompass.
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