Galen Data Panel on Regulatory and Clinical Considerations for SaMD

Galen Data has gathered the experts in one virtual room to discuss Regulatory and Clinical Considerations for SaMD for medical device innovators. Isabella Schmitt will be sharing a regulatory perspective for a medical device going through SaMD. She is contributing to this panel discussion with Karandeep Singh Badwal is an independent Quality & Regulatory consultant specializing within SaMD and AI medical devices.

Register for free to learn, interact, and engage industry experts in these three areas to learn about the synergies of these three critical spaces.  

Key Takeaways:

• What does the regulatory pathway look like for SaMD?
• What are some common mistakes that companies make and how to avoid them?
• How should you do clinical validation and testing for SaMD