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Navigating Vietnam's SaMD Cybersecurity Maze: A Pure Global Guide for MedTech Innovators in the ASEAN Market

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Manage episode 506343301 series 3684626
Content provided by Ran Chen. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Ran Chen or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.
In this episode of ASEAN MedTech Insights, we demystify the process of meeting cybersecurity requirements for Software as a Medical Device (SaMD) in Vietnam. While Vietnam lacks a specific cybersecurity law for MedTech, the regulatory expectations are high, embedded within the existing framework of Decree 98. We explore the essential documentation, from risk management to post-market surveillance, that manufacturers must prepare. We break down how to proactively demonstrate your SaMD's security to the Vietnamese authorities. This involves moving beyond simple compliance checklists and adopting a comprehensive lifecycle approach to cybersecurity, ensuring the safety and performance of your device in one of ASEAN's fastest-growing digital health markets. **Case Study Highlight:** Learn from the experience of an AI diagnostics company whose market entry into Vietnam was stalled. Their initial application failed to adequately address the risk of patient data breaches. Discover the specific steps they took in their technical dossier, including detailed threat modeling and penetration testing results, to finally secure regulatory approval. **Key Questions Answered in This Episode:** - Why doesn't Vietnam have a separate cybersecurity law for SaMD, and where are the requirements hidden? - What is the single most important document for proving your SaMD's security to Vietnamese regulators? - How can your 'Instructions for Use' document become a critical tool for cybersecurity compliance? - What are the specific expectations for monitoring and patching vulnerabilities after your product is on the market? - Is your software validation process, including penetration testing, robust enough for a successful submission? - How do you address risks like data breaches and unauthorized access within your ISO 14971 risk file? - What crucial details are regulators looking for in your post-market surveillance plan? Pure Global offers end-to-end regulatory consulting solutions for MedTech and IVD companies, combining local expertise with advanced AI to streamline global market access. Let us help you navigate the complexities of SaMD registration in Vietnam and beyond. Contact us at [email protected] or visit https://pureglobal.com/.
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34 episodes

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iconShare
 
Manage episode 506343301 series 3684626
Content provided by Ran Chen. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Ran Chen or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.
In this episode of ASEAN MedTech Insights, we demystify the process of meeting cybersecurity requirements for Software as a Medical Device (SaMD) in Vietnam. While Vietnam lacks a specific cybersecurity law for MedTech, the regulatory expectations are high, embedded within the existing framework of Decree 98. We explore the essential documentation, from risk management to post-market surveillance, that manufacturers must prepare. We break down how to proactively demonstrate your SaMD's security to the Vietnamese authorities. This involves moving beyond simple compliance checklists and adopting a comprehensive lifecycle approach to cybersecurity, ensuring the safety and performance of your device in one of ASEAN's fastest-growing digital health markets. **Case Study Highlight:** Learn from the experience of an AI diagnostics company whose market entry into Vietnam was stalled. Their initial application failed to adequately address the risk of patient data breaches. Discover the specific steps they took in their technical dossier, including detailed threat modeling and penetration testing results, to finally secure regulatory approval. **Key Questions Answered in This Episode:** - Why doesn't Vietnam have a separate cybersecurity law for SaMD, and where are the requirements hidden? - What is the single most important document for proving your SaMD's security to Vietnamese regulators? - How can your 'Instructions for Use' document become a critical tool for cybersecurity compliance? - What are the specific expectations for monitoring and patching vulnerabilities after your product is on the market? - Is your software validation process, including penetration testing, robust enough for a successful submission? - How do you address risks like data breaches and unauthorized access within your ISO 14971 risk file? - What crucial details are regulators looking for in your post-market surveillance plan? Pure Global offers end-to-end regulatory consulting solutions for MedTech and IVD companies, combining local expertise with advanced AI to streamline global market access. Let us help you navigate the complexities of SaMD registration in Vietnam and beyond. Contact us at [email protected] or visit https://pureglobal.com/.
  continue reading

34 episodes

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