Innovation and Regulation: How the AI Airlock Sandbox Can Help Medical Device Manufacturers!

Are you a developer or manufacturer of Artificial Intelligence (AI)-based medical devices?

Then you should know about the latest opportunity offered by MHRA, the UK’s regulatory agency. They have opened applications for the AI Airlock regulatory sandbox, created to tackle the regulatory challenges of AI medical devices (AIaMD).

💡What is the AI Airlock?

It’s an innovative sandbox designed to test and optimize the regulatory process, accelerating the entry of safe and innovative AI medical devices into the market for the benefit of patients and the NHS.

Why participate?

By joining the program, you’ll receive a personalized testing plan and collaborate closely with industry and regulatory experts. It’s a great opportunity to gain a better understanding of regulatory requirements and new data standards for AI medical devices, reducing risks before entering the market.

Who can apply?

The program is open until Monday, October 7th, and targets manufacturers with AI devices that can bring benefits to the NHS, represent innovations in the sector, and are ready to test their regulatory challenges.

If your AI device can make a difference, don’t miss this unique opportunity!

📅 Apply by October 7th to join the pilot program and shape the future of AI medical devices.

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