Our in-house team of regulatory affairs specialists and market access experts are strategically located across our offices in seven major Southeast Asian markets. With daily engagement with local medical device regulatory authorities and government departments, we provide real-time updates and expert guidance on medical device registration, importation procedures, and compliance requirements.

This direct, on-the-ground presence ensures you’re equipped with the latest insights to navigate the region’s complex and evolving regulatory landscape—especially during this period of increased post-market surveillance (PMS) and frequent changes in regulatory compliance.

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