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學術活動

國內學術活動

2026.12.03
台灣醫療科技展
2026.09.01
HTAsiaLink 2026 Conference
2026.07.15
BIO Asia–Taiwan 2026 亞洲生技大會
2026.06.16
愛爾蘭醫療科技創新生態系

國外研討會資訊

2026.11.19
【RAPS】Regulatory Challenges for Complex Devices, cATMPs, and Combination Products Delivery
2026.11.17
Combination Products Summit
2026.11.12
【RAPS】AI Medical Device Regulations: Global Strategies and Early Engagement
2026.11.08
ISPOR Europe 2026
2026.11.02
【RAPS】EU Medical Device Regulation 2017/745
2026.10.22
【RAPS】Health Canada's Medical Device Single Audit Program (MDSAP) Updates 2026
2026.10.20
【RAPS】Performance Studies Under IVDR: A Practical Guide for Pharma & Biotech Teams
2026.10.19
【RAPS】Clinical Evaluation for Medical Devices
2026.10.19
2026 TOPRA Symposium
2026.09.15
RAPS Convergence 2026
2026.09.06
ISPOR Asia Pacific Summit
2026.07.22
【RAPS】Practical EU MDR, UKCA, and FDA Risk Management & Labeling
2026.07.15
【RAPS】EU MDR/IVDR at the 10‑Year Mark: Proposed Reforms, Opportunities, and Challenges
2026.07.08
【RAPS】15 Years of Labeling: What's Changed and What's Next
2026.07.01
【RAPS】EU Deviations to IEC 61010-2-101: What IVD Manufacturers Need to Know
2026.06.26
【RAPS】Netherlands Chapter: Proposals MDR 2.0, IVDR 2.0 en Digital Omnibus
2026.06.26
【RAPS】AI Literacy for MedTech: Regulatory Augmented Intelligence
2026.06.23
【RAPS】Regulatory Pathways to Broaden Market Access
2026.06.22
【RAPS】Germany Chapter: Material Compliance and beyond
2026.06.18
【RAPS】Clinical Evaluation Submissions in The Fast-Changing MDR Environment
2026.06.17
【RAPS】IVDR Transition in 2026: Parallel Regulatory Planning for EU and US Market Entry
2026.06.17
【RAPS】AI Goes Wearable: From Algorithm Design to Patient Impact
2026.06.17
【RAPS】SaMD: What FDA Expects Vs What MDR Demands
2026.06.16
【RAPS】AI Governance in Life Sciences: ISO 42001
2026.06.15
MedTech Summit
2026.06.15
HLTH Europe 2026
2026.06.14
DIA 2026 Global Annual Meeting
2026.06.12
【RAPS】UK Medical Devices Legislation
2026.06.11
【RAPS】Mastering Notified Body Opinions for Drug-Device Combination Products under EU MDR 2017/745
2026.06.10
ARCS Australia
2026.06.09
【RAPS】Quality Conference
2026.06.04
【RAPS】How to Validate AI-Enabled, Non-Product Software
2026.06.04
【RAPS】MN Medical Devices Essentials 2026
2026.06.03
【RAPS】From Data Overload to Strategic Advantage: AI Solutions for Regulatory Excellence
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