『Pure Global’s ASEAN Playbook: Baking AMDD-Driven English Labeling from Singapore into Your Pan-Asia Dossier Strategy』のカバーアート

Pure Global’s ASEAN Playbook: Baking AMDD-Driven English Labeling from Singapore into Your Pan-Asia Dossier Strategy

Pure Global’s ASEAN Playbook: Baking AMDD-Driven English Labeling from Singapore into Your Pan-Asia Dossier Strategy

無料で聴く

ポッドキャストの詳細を見る

このコンテンツについて

 In this episode of ASEAN MedTech Insights, we explore the critical importance of a harmonized yet localized labeling strategy for medical device companies targeting Southeast Asia. While the ASEAN Medical Device Directive (AMDD) promotes English as the standard for technical dossiers, relying solely on an English-first approach tailored for markets like Singapore can create significant barriers to entry in countries with specific national language requirements, such as Thailand and Indonesia. We discuss how to move beyond a reactive, market-by-market approach to a proactive, pan-ASEAN strategy. Learn why integrating multilingual labeling into your core regulatory dossier from day one is essential for avoiding costly delays, redesigns, and logistical challenges, ultimately accelerating your multi-market launch and turning regulatory compliance into a powerful competitive advantage. **What You'll Learn:** * Why can an English-only label strategy successful in Singapore become a major roadblock in other ASEAN markets? * What are the hidden costs and delays of overlooking local language requirements in countries like Thailand or Vietnam? * How does the ASEAN Medical Device Directive (AMDD) promote harmony while still allowing for critical national differences in labeling? * When is the right time to integrate multilingual labeling into your dossier—before or after your first ASEAN market entry? * How can a unified dossier strategy that anticipates local needs save you months, or even years, in your regional expansion timeline? * What specific steps should be included in your Quality Management System to manage a pan-ASEAN labeling process effectively? * Why is a local in-country representative essential for navigating these nuanced labeling norms? At Pure Global, we specialize in creating seamless regulatory strategies that blend global standards with local expertise. Our end-to-end solutions for MedTech and IVD companies leverage advanced AI and data tools to streamline market access across more than 30 countries, including the entire ASEAN region. Let us help you build a dossier that works everywhere. Contact us at info@pureglobal.com or visit https://pureglobal.com/ to learn more.
まだレビューはありません