Speed your medical devices to market with this complimentary guide which takes you step by step through the process of submitting your medical devices for approval from the FDA.
As a leader in third party testing and certification, Intertek’s industry experts developed this guide to simplify the complex process to submit your medical devices to the FDA and provide an in-depth understanding of all that is involved, including:
- Classifying your device
- Identifying the correct premarket submission
- Preparing the premarket submission
- Submitting to the FDA
- Establishing a registration and device listing