Good Clinical Practice ISO 14155 for Medical Devices

Welcome to this complete edition of the ISO 14155 GCP course on Clinical Investigations with Medical Device. This course offers the first professional, detailed course for Investigators, Study Coordinators, Sponsors, Clinical Project Managers, Monitors and any other Clinical Study staff requiring knowledge in GCP for a successful execution your clinical trials with Medical Devices. This GCP course is maintained up-to-date with upcoming revisions as they become available.

My name is Dr. Vincent Baeyens PhD, I have more than 20 years of experience in running Clinical Trials in Global and mid-size Pharma, and Biotech settings. I have worked with most of the Global as well as several niche CROs and I am also an expert in CRO Management and Oversight, budgeting and Risk Management.

In this course, you will be able to understand ISO GCP requirements to plan, conduct, clinical trials with Medical Devices in humans. We will review the role and responsibilities of the key stakeholders. To facilitate the learning of beginner students, the course has been broken up on purpose in several small lectures.

This course will provide you with a strong support to prepare for successful regulatory GCP inspections and audits. I will lead you step-by-step through the ISO 14155 GCP, and you will learn and understand:What is a Medical DeviceRegulatory framework of ISO 14155Common ISO GCP audit and inspection findings in clinical investigations (sponsor/investigator)Scope of ISO 14155ISO 14155 Good Clinical Practice principlesThe responsibilities of ethics committees, principle investigators and sponsorHow to effectively plan a Clinical InvestigationWhat are the key steps to conduct a Clinical InvestigationWhat to focus upon in order to be audit and inspection-readyReflect upon potential deviations to ISO 14155 GCPs and possible action planPlease note that, for copyright reasons, I am not allowed to share the copy of the ISO 14155 norm. A final Quiz at the end of the course will consolidate your knowledge.