REGULATORY
RMPs Required for Generics when RMPs Submitted for Original Products: Health Ministry
Generic makers are likely to be required to submit Risk Management Plans (RMPs) for generics if RMPs have already been filed for their original products, based on the health ministry’s plan. The ministry’s Pharmaceutical and Food Safety Bureau is now…
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I recently sat down with one of the leading medical directors in Japan to discuss the critical evolution of the medical science liaison (MSL) role.The MSL has transformed from a scientific resource into a strategic partner essential for successful product…





