A key problem in transferring new MR sequences into clinical practice is the complexity of the approval processes. Sequences are often programmed directly in the device manufacturers' proprietary development environments and approved together with the respective hardware.
"For specialized or novel approaches, this barrier is often difficult to overcome," says project manager Hoinkiss. "Our aim is to simplify and, in a sense, democratize the certification process, making it more accessible for third-party providers."
This is where the gammaSTAR platform comes in. It enables MR sequences to be developed, simulated, and reconstructed in a manufacturer-neutral manner. The sequences can then be executed on different MRI scanners via standardized interfaces.
"We designed the platform in such a way that MR sequences already meet a quality standard that fundamentally allows for subsequent medical device approval," explains Dr. Nora-Josefin Breutigam, responsible for quality and partner management at Fraunhofer MEVIS.