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