Sign up here to join the study. You qualify if:
- You work in the medical device field
- Your work involves dealing with regulations, for example QA/RA, R&D
- You have at least 1 year of experience in this field
You will receive access to dedicated AI models for MDR, IVDR and FDA regulations and be trained on them as part of the study. The expected time investment is about 2 hours.
After you sign up, our team will be in touch to let you know if you’ve been included in the study cohort. Thank you in advance!