『Unlocking ASEAN MedTech Markets: A Pure Global Deep Dive into the Common Submission Dossier Template (CSDT) for Singapore, Malaysia, and Beyond.』のカバーアート

Unlocking ASEAN MedTech Markets: A Pure Global Deep Dive into the Common Submission Dossier Template (CSDT) for Singapore, Malaysia, and Beyond.

Unlocking ASEAN MedTech Markets: A Pure Global Deep Dive into the Common Submission Dossier Template (CSDT) for Singapore, Malaysia, and Beyond.

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 In this episode of ASEAN MedTech Insights, we explore the ASEAN Common Submission Dossier Template (CSDT). Designed to unify medical device registration across Southeast Asia, the CSDT promises a simplified path to market. However, manufacturers often discover that a "common template" does not mean a common process. We uncover the practical challenges and country-specific hurdles that can delay or derail your expansion plans. We dive into the critical differences in how countries like Singapore, Malaysia, and Thailand interpret and implement the CSDT. We share a real-world case study of a MedTech company that prepared a flawless CSDT based on their CE marking file, only to face unexpected requirements for specific certificates in Malaysia and mandatory local language translations in Thailand. These seemingly small details led to significant budget overruns and a launch delay of several months, highlighting the costly gap between regulatory theory and market reality. Key Questions Answered in This Episode: - What exactly is the ASEAN CSDT and which countries have adopted it? - Is the CSDT a true "one-and-done" submission for the entire ASEAN region? - How do CSDT requirements in Singapore differ from those in Malaysia or Thailand? - What are the most common and costly mistakes companies make when preparing their dossier? - Why is your existing CE or FDA technical file not enough for a successful ASEAN submission? - What are the specific local language and labeling requirements you cannot afford to ignore? - Why is an in-country representative still essential despite a harmonized template? - How can you anticipate and budget for hidden costs like translation and additional certifications? Navigating the complexities of ASEAN's regulatory landscape requires more than just a template. Pure Global offers end-to-end regulatory consulting solutions for MedTech and IVD companies, combining local expertise with advanced AI and data tools to streamline global market access. We act as your local representative in over 30 markets, ensuring your submissions meet the nuanced requirements of each country from the start. Stop letting unforeseen hurdles slow your growth. Contact Pure Global for a tailored market access strategy at info@pureglobal.com or visit https://pureglobal.com/ to learn more.
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