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Rising APAC Device MnA Demonstrates The Need For Regulatory Strategy

This article was originally published in SRA

Executive Summary

The number of M&A deals across Asia Pacific is increasing rapidly. But demonstration of product regulatory compliance is often not transferrable between APAC countries. How do you overcome this and other regulatory hurdles during your M&A deal-making? In this article, Ee Von Teo and Daniel Tan, together with their colleagues*, explain how to manage this dynamic new market opportunity. They also give a breakdown of the different medical device regulatory regimes in APAC and the transferability of registrations and licences by individual countries.




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