TTP plc

Integrating sensing into minimally invasive medical devices is more than a sensor-selection challenge. Explore how a system architecture approach, considering device mechanics, electronics, packaging and calibration, can help development teams achieve clinically useful measurements without compromising device performance, manufacturability or reliability.

For active medical implants with long conductive leads, assessing MRI-induced RF heating can quickly become a significant development bottleneck. Explore how computational transfer-function modelling can streamline ISO 10974 Tier 3 assessment, reduce repeated phantom testing and enable faster design iteration.

Whether you’re exploring how ultrasound could fit into a new medical product, or already developing ultrasound systems yourself, we’ve drawn on eight years’ experience developing a software-defined ultrasound system. We share lessons in modularity, synchronisation, scalability, integration and designing for experimentation.

Reliable Bluetooth connectivity from inside the body creates difficult trade-offs between antenna size, power, signal strength and tissue effects. See how modelling, prototyping and testing can be combined to develop robust wireless performance within the constraints of an implantable continuous glucose monitor. Explore more: https://lnkd.in/eJUwVd89/?utm_campaign=HT-MedTech-Guides-StartUps&utm_source=linkedin&utm_medium=paid&utm_id=1239091324&hsa_acc=517471480&hsa_cam=1239091324&hsa_grp=905561354&hsa_ad=1611728364&hsa_net=linkedin&hsa_ver=3

Connecting a medical device to the cloud creates an evolving ecosystem spanning device software, connectivity, cybersecurity, data and long-term operations. Discover the engineering challenges that often emerge beyond the prototype – and how to design for them from the outset.

Regulatory requirements don't have to be a significant burden - they can help guide development decisions and reduce costly rework. Our guide explores how regulatory thinking can: ▪️Inform early design and architecture decisions ▪️Reduce the risk of costly redesign ▪️Help create a more credible path towards clinical studies and commercialisation