One of the subscribers on our KZfaq channel requested this video topic. They submitted an email requesting that we explain the guidelines for launching a medical device clinical study in the USA. They also requested an explanation of the timeline and the documentation required. We won’t have time to get into the details of an IDE submission, but we will provide links in the video’s description for where to find the details of what is required for an IDE for a pivotal study, where to find CDRH Learn presentations specific to clinical studies, and where to find information about Early Feasibility Studies (EFS). We will also discuss other types of studies that do not require an IDE.
CDRH Learn ➤ www.fda.gov/training-and-cont...
IDE Guidance ➤ www.fda.gov/medical-devices/i...
IDE Guidance for EFS & FIH Studies ➤ www.fda.gov/media/81784/download
ISO 14155:2020 Standard ➤ www.evs.ee/en/evs-en-iso-1415...
We also sell a clinical procedure (SYS-009) that provides high-level guidance on the steps required for a clinical study ➤ medicaldeviceacademy.com/clin...