On September 30, 2026, MEDIDECT delivered a series of professional lectures at the Medical Device Clinical Trials and Regulatory Affairs Practical Workshop, organized by the Leading Research Center for Multimodal Contactless Sensing for Lifelog Applications (RLRC).
The workshop was held at the Daegu Marriott Hotel from September 30 to October 1, 2026, with the aim of strengthening participants’ practical understanding of medical device clinical trials and regulatory requirements.
Nammi Park, CEO of MEDIDECT, led the clinical trial training sessions on the first day, covering the following topics:
- Medical device clinical trial regulations and Good Clinical Practice (GCP)
- Clinical trial protocols, informed consent forms, and Institutional Review Board (IRB) review
- Medical device clinical trial management, data management, and study conduct
- Clinical trials for digital medical devices
Through practical insights and industry experience, MEDIDECT shared essential considerations for planning, managing, and conducting medical device clinical trials.
MEDIDECT remains committed to supporting innovative medical technologies through specialized clinical development services, regulatory expertise, and professional education.