Symposiums/Seminars for Regulatory Affairs Professionals
Our symposiums/seminars help regulatory affairs professionals in charge of quality, develpment, approval application, post-market surveillance and regulatory affairs etc. of pharmacueticals nad medical devices to improve ability and gain a path to success. And another aim of our symposiums/seminars is to promote Japanese regulatory science of pharmaceuticals and medical devices. There are five categories of general science/technology, development, post-marketing, quality and medical devices in our symposiums/seminars. We pick up important and special themes timely, and invite professional speakers from industries, MHLW (Ministry of Health, Labour and Welfare), PMDA (Pharmaceuticals and Medical Devices Agency) and academia for lectures. After lectures we have enough time to discuss and search for the problems.
Lectures Classes on Recent Development of Pharmaceutical Regulations
Speakers from PMDA, NIHS (National Institute of Health Sciences) and JPMA (Japan Pharmaceutical Manufacturers Association) report the results of the latest meetings in ICH. Specialists of MHLW, PMDA and NIHS explain topics of Japanese Pharmacopoeia, too.
Technical Trainings on General Test Methods in Japanese Pharmacopoeia
We hold technical trainings about general experiments based on Japanese Pharmacopoeia (e.g. a test method for endotoxin, validation of an analysis, and a measuring method by NMR etc.).
(Last update: 20-June-2011)