The Ministry of Health, Labor and Welfare (MHLW) will require regulatory filing for generic drugs in the Common Technical Document (CTD) format as a basic rule, beginning on March 1, 2017.The new requirement will exclude biologics, radiopharmaceuticals, recombinant products, cell…
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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.…





