This episode of ASEAN MedTech Insights provides a deep dive into the specific requirements for registering Software as a Medical Device (SaMD) in the Philippines. We explore the critical steps from risk classification and dossier preparation to the final submission process, offering practical insights for MedTech innovators targeting this key ASEAN market. Imagine you've developed a groundbreaking AI diagnostic app, poised to revolutionize patient care. You're targeting the fast-growing Philippine market, but the regulatory maze is daunting. You're unsure how to classify your SaMD, struggling to compile the ASEAN Common Submission Dossier Template (CSDT), and you lack the mandatory local representative required for submission. Every delay pushes back your market entry, drains resources, and jeopardizes your competitive edge. Key Takeaways: 1. What are the four risk classifications for SaMD in the Philippines and how do they impact your registration strategy? 2. Why is the ASEAN Common Submission Dossier Template (CSDT) a game-changer for regional expansion? 3. Is a local authorized representative mandatory for submitting your SaMD application? 4. What specific documentation does the Philippine FDA expect for a software cybersecurity plan? 5. How can approval in one ASEAN country potentially fast-track your registration in the Philippines? 6. What is the difference in submission procedures for low-risk versus high-risk SaMD? 7. What are the most common pitfalls that lead to submission delays and rejections? Pure Global offers end-to-end regulatory consulting solutions for MedTech and IVD companies. We combine local expertise with advanced AI and data tools to streamline global market access. Let us be your local representative and strategic partner in navigating the complexities of the Philippine market. Contact us at [email protected] or visit https://pureglobal.com/ to learn more.