加入會員 聯絡學會
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
2026.07.10
進入美國市場：每位生醫創新者的必備知識
2026.07.02
AI 醫療落地卡關大解密：法規、安規、資安到風險治理如何不踩雷
2026.06.25
從創新板到全球授權：漢康生技打造國際新藥公司的實戰經驗

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
2026.09.25
Regulatory Perspectives on Herbal Medicinal/Botanical Drug Product Development – Joint FDA/EMA Workshop
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
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