『Pure Global's ASEAN MedTech Insights: Mastering Vietnam's Regulatory Maze from Decree 98 to Decree 07 for Market Success.』のカバーアート

Pure Global's ASEAN MedTech Insights: Mastering Vietnam's Regulatory Maze from Decree 98 to Decree 07 for Market Success.

Pure Global's ASEAN MedTech Insights: Mastering Vietnam's Regulatory Maze from Decree 98 to Decree 07 for Market Success.

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 In this episode of ASEAN MedTech Insights, we unravel the complex regulatory web governing medical devices in Vietnam. We provide a deep dive into the foundational Decree 98/2021, the detailed implementation guide of Circular 05/2022, and the critical deadline extensions provided by Decree 07/2023. This is a must-listen for any MedTech company currently in or planning to enter the fast-growing Vietnamese market. We break down what these changes mean for your product registration, documentation, and overall market access strategy, moving beyond legal jargon to provide actionable insights. Imagine being a manufacturer of a Class C diagnostic device, with your Vietnamese import license about to expire. The new regulations demand a complex technical dossier in a format your team has never prepared, and the deadline is fast approaching. A single mistake in the submission could lead to rejection, halting your sales and severing relationships with local distributors. This episode walks you through how to navigate this exact scenario. Key Takeaways: * What fundamental shift did Decree 98/2021 introduce to Vietnam's medical device approval process? * How does Circular 05/2022 specify the dossier requirements for high-risk devices? * Why was Decree 07/2023 considered a critical lifeline for foreign manufacturers? * What are the most common pitfalls when preparing a Common Submission Dossier Template (CSDT) for the Vietnamese authorities? * How can you effectively manage the transition from an old import license to a new marketing authorization number? * What are the current, final deadlines that your company absolutely cannot miss? * What role does a local license holder play under the new regulatory framework? Navigating ASEAN's regulatory environment requires specialized local knowledge and a global perspective. Pure Global offers end-to-end regulatory consulting solutions for MedTech and IVD companies, leveraging local expertise and advanced AI tools to streamline your market access. From initial regulatory strategy and technical dossier submission to post-market surveillance, we act as your single partner for multiple markets. Contact us for a strategic consultation at info@pureglobal.com or visit https://pureglobal.com/.
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