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 Forest brand of ferrous fumarate Drug Master File in Japan (Forest brand of ferrous fumarate JDMF) empowers Forest brand of ferrous fumarate 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 Forest brand of ferrous fumarate JDMF during the approval evaluation for pharmaceutical products. At the time of Forest brand of ferrous fumarate 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 Forest brand of ferrous fumarate suppliers with JDMF on PharmaCompass.