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