EUDAMED Journey
Your Journey to EUDAMED SubmissionÂ
As the September 2022 deadline to comply with EU MDR quickly approaches, it’s time to take charge of your regulatory compliance strategy and compete to win in the new medical device regulatory climate.
At Innovit, we help companies achieve EU MDR compliance and drive innovation with solutions and processes. Explore the steps to adapt to this new normal across the industry and ensure EUDAMED compliance.
Your Journey to EUDAMED Submission
Step 1
Secure Executive Sponsorship
Step 2
Obtain an SRN
Step 3
Prepare and Validate
Step 4
Determine 3rd Part Access
Step 5
Specify Actor's M2M submission
Step 6
Generate an Access Token
Step 7
Device Submissions via your Access Point
Step 8
Celebrate your success!