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學術活動

國內學術活動

2026.12.03
台灣醫療科技展
2026.07.15
BIO Asia–Taiwan 2026 亞洲生技大會
2026.04.21
諾貝爾大師在清華 Industry Forum Registration
2026.03.26
2026邁向上市之路-AI、生技醫療與高科技產業資安治理與個資合規交流會
2026.03.25
Biologics World Taiwan 2026

國外研討會資訊

2026.11.08
ISPOR Europe 2026
2026.09.15
RAPS Convergence 2026
2026.06.14
DIA 2026 Global Annual Meeting
2026.06.04
【RAPS】How to Validate AI-Enabled, Non-Product Software
2026.06.02
FDA/MHRA/Health Canada Symposium: Regulatory perspectives in good clinical practice, bioequivalence and good pharmacovigilance practice
2026.05.18
【RAPS】Risk Management for Medical Devices
2026.05.17
ISPOR 2026
2026.05.13
【RAPS】The Role of the PRRC Under the MDR and IVDR
2026.05.11
【RAPS】Biologics CMC: Regulatory Challenges and Trends
2026.05.05
RAPS Euro Convergence 2026
2026.04.30
【RAPS】The Unseen Risk Between MI and PV
2026.04.29
【RAPS】From Signal to Submission: Steering Biomarker Driven Development Through the EU Regulatory Landscape
2026.04.28
【RAPS】Demystifying the Use-Related Risk Analysis (URRA) in Human Factors Validation Programs
2026.04.27
【RAPS】Streamlining Multi-Region Submissions: MDR, FDA, and EU AI Act
2026.04.21
【RAPS】Regulatory Requirements for Investigational Combination Products in Cell and Gene Therapy - A Global CMC Perspective
2026.04.20
【RAPS】Clinical Evaluation for Medical Devices
2026.04.02
【RAPS】Beyond Submission Assembly: Managing the Full Regulatory Review Lifecycle
2026.03.24
DIA Europe Annual Meeting 2026
2026.03.11
【RAPS】AI Navigation for Regulatory Professionals in 2026: Approaches, Tools and Practical Thinking
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