Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
BUSINESS
DSP’s US Subsidiary Sunovion Announces FDA Acceptance of NDA Resubmission for Epilepsy Treatment Stedesa
Dainippon Sumitomo Pharma’s US subsidiary Sunovion Pharmaceuticals announced on February 27 (US time) that the US FDA has accepted the company’s new drug application (NDA) resubmission for Stedesa (eslicarbazepine acetate) for use in patients with epilepsy. Sunovion submitted the original…
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A few weeks ago, I had coffee with a very talented executive. Let’s call him Kenji. He has a great job, a big salary, and a solid team. But he was unhappy. He felt bored and wanted a new challenge.…
Japan’s Central Social Insurance Medical Council (Chuikyo) on November 5 approved the reimbursement listing for a slate of new medicines,…
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