內 容
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中國醫藥大學附設醫院 - 臨床試驗中心將舉辦「性別考量、研究倫理與受試者保護訓練課程」課程，敬邀 貴機構有興趣者踴躍報名參加，惠請 查照轉知。
說明：
一、本課程採用Cisco Webex授課軟體進行同步線上教學。
二、課程資訊：
(一)課程日期：115年12月02日(星期三)
(二)課程時間：下午01:30 至05:30。
(三)報名網址：https://edu.cmuhctc.tw/activity-page/1/922。
(四)參加對象：臨床試驗主持人、研究護理師、IRB委員及行政人員，以及藥廠、CRO之臨床、法規、品質與藥物安全等專業人員；亦適合對研究倫理、受試者保護及臨床研究相關議題有興趣之人員。
(五)符合「參與課程時間超過200分鐘」、「課後測驗達80分及格」及「限時完成滿意度調查」者，將核發4小時GCP學分。
(六)課程報名費用：840元，報名繳款前請務必審慎確認可否出席；完成課程繳費後，若因故無法參加，恕不受理取消報名、異動、轉讓他人及退款申請。
The Clinical Trial Center of China Medical University Hospital will host a training course titled "Gender Considerations, Research Ethics, and Subject Protection." We cordially invite interested individuals from your institution to register and participate. We would appreciate it if you could disseminate this information to the relevant parties.
Description:
I. This course will be conducted via synchronous online instruction using the Cisco Webex platform.
II. Course Information:
(1) Date: Wednesday, December 2, 2026.
(2) Time: 01:30 PM to 05:30 PM.
(3) Registration Link: https://edu.cmuhctc.tw/activity-page/1/922.
(4) Target Audience: Principal Investigators, Research Nurses, Institutional Review Board (IRB) members, and administrative staff; professionals in clinical, regulatory, quality, and pharmacovigilance departments of pharmaceutical companies and Contract Research Organizations (CROs); and individuals interested in research ethics, subject protection, and clinical research-related issues.
(5) Participants who meet the requirements of "attending the course for more than 200 minutes," "achieving a passing score of 80% on the post-course assessment," and "completing the satisfaction survey within the designated time limit" will be awarded 4 hours of Good Clinical Practice (GCP) credits.
(6) Registration Fee: NT$840. Please ensure your availability before proceeding with the payment. Once the payment is completed, no requests for cancellation, modification, transfer to others, or refunds will be accepted. |
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