Start planning for your medical device registration (MDMA) in the SFDA by conducting an accurate gap analysis on a comprehensive list of requirements, with high-value notes from our experts. Also, you may want to read about how to appoint an authorized representative or change your current one in Saudi Arabia to perform the registration on your behalf.
You will receive in this file:
- List of 35+ files that are required in your medical device technical file.
- Valuable notes on every point.
- Custom requirements for SFDA
- Corresponding risk classes in Saudi Arabia
Fill the form and receive the downloadable sheet instantly.