Product context matters. Explore the technology experience that informs the Crossroads practice.
Experience by technology
These areas describe background experience, not a blanket commitment to support every product. Suitability for your device is established in the initial discussion.
Software as a medical device, patient monitoring, and cardiology monitoring systems.
Software-only products and connected monitoring systems bring together software changes, intended use, and ongoing product maintenance.
Ultrasound, cardiovascular devices, endoscopy, and visualization systems.
Imaging and interventional products require attention to product classification, supporting documentation, and the implications of design changes.
Respiratory therapy, ventilators, and drug-delivery devices.
Delivery systems and respiratory devices can raise questions about intended use, applicable standards, and the relationship between device and therapy.
Single-use products, radiation treatment, and mobility assistance.
The practice also draws on background experience with disposable products, active and non-active devices, and treatment systems. Fit for a specific technology is discussed before work is agreed.
Start a conversation
Tell us about your product, your priorities, and the question ahead. A brief, non-confidential overview is enough to begin.
Contact Crossroads