Management software

monitoringmedicalcentralized

Simplify Compliant Medical Software Development Go from SaMD concept to execution with an
IEC-62304-compliant software suite that guides
you through all the steps required for certification. Mia-Care’s Platform for Software as a Medical Device enables MedTech companies to bring digital-compliant solutions for medical software to the market. GET RID OF Regulation Pitfalls Certification Hurdles Development Extra Costs Mia-Care Key Features for SaMD Development Centralized Governance Leverage an Internal Developer Platform to see SaMD projects’ development status utterly. High Automation Eliminate errors and improve efficiency by automating testing and technical documentation creation. Regulatory Compliance Manage the software lifecycle through regulated and ISO 13485 and 62304 compliant processes. Guided development experience Eliminate SaMD development complexity and allow developers to focus on software quality. BRING VALUE AT ALL ORGANIZATION LEVELS For Developers Developers can manage the software lifecycle and IT infrastructure in a simplified, controlled, and guided way while complying with industry regulations and predefined software specifications. For Product Owners Product Owners can manage the product development specifications and risks, monitor progress and adherence to industry regulations, and manage the documentation for certifying bodies. For Tech Leaders Technical leaders can follow the team’s work throughout the software lifecycle and fully control software dependencies, release management, and software monitoring in production.