Medical Apps & Web Software

Camgenium's transformative 'no-code' regulatory compliant platform enables MedTech innovators to rapidly create medical-grade apps and web software to ISO 13485 Medical device standards for Class I/IIa intended use. We also produce bespoke applications up to Class III intended use.

Medical device software development is expensive, slow, and can be risky. Camgenium's pre-built software solution reduces development cost, time to market and risk, by complying with medical quality and software standards that are mandated worldwide.

Camgenium's platform enables STEM engineers to build regulatory compliant products in a small fraction of the time needed for bespoke coding by using validated, compliant pre-built components.

AI models and other algorithms or bespoke code modules can be included in applications created by the platform's drag and drop editor. Likewise the platform can be interfaced to third party APIs, particularly useful for interoperability. This wide range of functionality allows the platform to radically simplify the creation of new medical device-grade products and prototypes.

Camgenium's software also supports complex triggers from both web and mobile controls that will send alerts, messaging and force conditional navigation through an application. This allows alerting like Email, Push and SMS notifications to be set up generically.

The platform enables sophisticated and highly granular group permissions. These permissions can be very useful in applications where different types of users have restrictions on the data they may see, such as patient apps and specialised websites for clinicians, researchers, and administrators.

Camgenium's no-code platform features built-in design tools allowing for complex applications to be built using drag and drop design methods with minimal need for bespoke coding. The platform leverages Camgenium's years of expertise gained in the development of quality systems and medical products that has been captured in its code base to ensure immediate compliance with regulations. The system automatically documents changes, allowing affordable iterative product development that results in more usable products. All prototypes built on the platform maintain a full, auditable design history.

Camgenium's 'no-code' software platform enables the rapid development of clinical trial apps and web software. The platform's inherent audit capabilities ensure compliance with Good Clinical Practice (GCP) and enable applications built to medical device standards.

Apps can be readily built that collect information not just from questionnaires but also about users' real-time interaction with the app itself. This innovation was conceived from developing products for neurodivergent and brain-injured patients and allows more nuanced data to be collected than just the answers to a questionnaire. Around twenty different types of user action can be determined and captured as the application is used. For example, the exact position and timing of a user touching the screen and the order in which the user navigates an application can provide valuable data on subjects with neurological conditions.

Camgenium's platform also enables rapid production of apps that are interfaced, for example via BLE, to devices capturing biometric information

All data captured by the platform is also stamped with detailed versioning information for the application. This provides the objective evidence to enable formal review and audit of screens and database schemas.

If your requirement falls outside of our platform capabilities, our team of expert engineers can create bespoke regulatory compliant mobile apps and web applications utilising the latest technologies.

Ready to build your medical-grade app? Contact our experts today.