Master Laboratory Co., Ltd. was honored to be invited by the Taiwan Food and Drug Administration (TFDA) to contribute its expertise to the “Comprehensive Professional Review Training Program for Medical Devices” in conjunction with the “Medical Device Biocompatibility Assessment and Case Study Sharing.”
Our team shared practical experience and real-world case studies, providing industry professionals actionable insights on biocompatibility testing and evaluation to support medical device safety, quality, and regulatory compliance.
110 年 03 月 26 日(星期五) 09:10 ~ 16:30 於衛生福利部食品藥物管理署 舉行「醫療器材全方位專業審查訓練計畫」暨「醫療器材生物相容性評估及試驗案例分享」，誠摯邀請瑞德生物科技股份公司各位業界先來臺授課。
