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 Aluminosilicic acid (HAlSiO4), magnesium salt Drug Master File in Japan (Aluminosilicic acid (HAlSiO4), magnesium salt JDMF) empowers Aluminosilicic acid (HAlSiO4), magnesium salt 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 Aluminosilicic acid (HAlSiO4), magnesium salt JDMF during the approval evaluation for pharmaceutical products. At the time of Aluminosilicic acid (HAlSiO4), magnesium salt 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 Aluminosilicic acid (HAlSiO4), magnesium salt suppliers with JDMF on PharmaCompass.