MEDICA 2025 (November 17–20) is the essential convergence point for healthcare technology. We believe the future of health is connected, but the path to compliance shouldn't take years or deplete budgets. Our presence at MEDICA is focused on demonstrating how to drastically reduce the time and cost associated with launching certified remote patient monitoring (RPM) solutions.
We invite developers, digital health pioneers, and medical device manufacturers to visit us in The Startup Park at Hall 12/SD19-13 in Düsseldorf.
The Actimi Platform: Reducing Your Operational Cost and Risk
Launching a certified remote patient monitoring (RPM) solution means taking on massive risk and unpredictable timelines. Our solution is an API-first Medical Backend as a Service—an established, compliant foundation ready for your product.
We assume the operational overhead and regulatory risk associated with:
Compliance Maintenance: We handle continuous ISO 13485 and ISO 27001 quality management and adaptation to evolving MDR requirements, saving your internal legal and quality teams immense effort.
Interoperability: Our platform is built on the industry standard HL7 FHIR, guaranteeing secure, standardized data flow with medical devices and existing hospital EHR systems.
Speed to Market: By eliminating infrastructure development and compliance delays, our partners achieve up to a 70% reduction in the development timeline compared to building from scratch.
This allows you to allocate your R&D budget directly to features that drive patient engagement and revenue, rather than back-end infrastructure.
SIGNALS: The Strategic Shortcut to MDR IIa
For any digital tool that analyzes patient data to assist in diagnosis or risk management, MDR Class IIa certification is legally required. This typically blocks market entry for 18-24 months and incurs hundreds of thousands in direct compliance costs.
Actimi SIGNALS is the solution: our pre-certified MDR IIa Medical Analysis API.
By integrating SIGNALS, your business instantly acquires the certified analysis capability it needs. This means you can:
Fast-Track Revenue: Skip years of regulatory backlog and start generating revenue sooner.
Ensure Stability: Access a robust, pre-validated medical analysis engine for all vital parameters.
Control Costs: Replace massive, unpredictable internal certification costs with a manageable, predictable service integration fee.
SIGNALS is not just technology; it helps you smoothen the way to a fast and MDR compliant market entry.
For Business Leaders and developers:
We look forward to discussing the concrete financial and operational advantages of using a pre-certified platform.
📍 VISIT US AT: Hall 12/SD19-13, Messe Düsseldorf
At our stand, we will highlight the immediate business value through:
API-First Platform in Action: A demonstration of how our API platform can serve as the backend for your medical application.
MDR IIa Certification Updates: How leveraging our certified services dramatically reduces regulatory risk and speeds up product launches.
HiBaby App Demonstration: A successful, real-world example of compliant, scalable patient monitoring (for maternal and infant care) built entirely on our platform.
MEDICA 2025 (November 17–20) is the essential convergence point for healthcare technology. We believe the future of health is connected, but the path to compliance shouldn't take years or deplete budgets. Our presence at MEDICA is focused on demonstrating how to drastically reduce the time and cost associated with launching certified remote patient monitoring (RPM) solutions.
We invite developers, digital health pioneers, and medical device manufacturers to visit us in The Startup Park at Hall 12/SD19-13 in Düsseldorf.
The Actimi Platform: Reducing Your Operational Cost and Risk
Launching a certified remote patient monitoring (RPM) solution means taking on massive risk and unpredictable timelines. Our solution is an API-first Medical Backend as a Service—an established, compliant foundation ready for your product.
We assume the operational overhead and regulatory risk associated with:
Compliance Maintenance: We handle continuous ISO 13485 and ISO 27001 quality management and adaptation to evolving MDR requirements, saving your internal legal and quality teams immense effort.
Interoperability: Our platform is built on the industry standard HL7 FHIR, guaranteeing secure, standardized data flow with medical devices and existing hospital EHR systems.
Speed to Market: By eliminating infrastructure development and compliance delays, our partners achieve up to a 70% reduction in the development timeline compared to building from scratch.
This allows you to allocate your R&D budget directly to features that drive patient engagement and revenue, rather than back-end infrastructure.
SIGNALS: The Strategic Shortcut to MDR IIa
For any digital tool that analyzes patient data to assist in diagnosis or risk management, MDR Class IIa certification is legally required. This typically blocks market entry for 18-24 months and incurs hundreds of thousands in direct compliance costs.
Actimi SIGNALS is the solution: our pre-certified MDR IIa Medical Analysis API.
By integrating SIGNALS, your business instantly acquires the certified analysis capability it needs. This means you can:
Fast-Track Revenue: Skip years of regulatory backlog and start generating revenue sooner.
Ensure Stability: Access a robust, pre-validated medical analysis engine for all vital parameters.
Control Costs: Replace massive, unpredictable internal certification costs with a manageable, predictable service integration fee.
SIGNALS is not just technology; it helps you smoothen the way to a fast and MDR compliant market entry.
For Business Leaders and developers:
We look forward to discussing the concrete financial and operational advantages of using a pre-certified platform.
📍 VISIT US AT: Hall 12/SD19-13, Messe Düsseldorf
At our stand, we will highlight the immediate business value through:
API-First Platform in Action: A demonstration of how our API platform can serve as the backend for your medical application.
MDR IIa Certification Updates: How leveraging our certified services dramatically reduces regulatory risk and speeds up product launches.
HiBaby App Demonstration: A successful, real-world example of compliant, scalable patient monitoring (for maternal and infant care) built entirely on our platform.
MEDICA 2025 (November 17–20) is the essential convergence point for healthcare technology. We believe the future of health is connected, but the path to compliance shouldn't take years or deplete budgets. Our presence at MEDICA is focused on demonstrating how to drastically reduce the time and cost associated with launching certified remote patient monitoring (RPM) solutions.
We invite developers, digital health pioneers, and medical device manufacturers to visit us in The Startup Park at Hall 12/SD19-13 in Düsseldorf.
The Actimi Platform: Reducing Your Operational Cost and Risk
Launching a certified remote patient monitoring (RPM) solution means taking on massive risk and unpredictable timelines. Our solution is an API-first Medical Backend as a Service—an established, compliant foundation ready for your product.
We assume the operational overhead and regulatory risk associated with:
Compliance Maintenance: We handle continuous ISO 13485 and ISO 27001 quality management and adaptation to evolving MDR requirements, saving your internal legal and quality teams immense effort.
Interoperability: Our platform is built on the industry standard HL7 FHIR, guaranteeing secure, standardized data flow with medical devices and existing hospital EHR systems.
Speed to Market: By eliminating infrastructure development and compliance delays, our partners achieve up to a 70% reduction in the development timeline compared to building from scratch.
This allows you to allocate your R&D budget directly to features that drive patient engagement and revenue, rather than back-end infrastructure.
SIGNALS: The Strategic Shortcut to MDR IIa
For any digital tool that analyzes patient data to assist in diagnosis or risk management, MDR Class IIa certification is legally required. This typically blocks market entry for 18-24 months and incurs hundreds of thousands in direct compliance costs.
Actimi SIGNALS is the solution: our pre-certified MDR IIa Medical Analysis API.
By integrating SIGNALS, your business instantly acquires the certified analysis capability it needs. This means you can:
Fast-Track Revenue: Skip years of regulatory backlog and start generating revenue sooner.
Ensure Stability: Access a robust, pre-validated medical analysis engine for all vital parameters.
Control Costs: Replace massive, unpredictable internal certification costs with a manageable, predictable service integration fee.
SIGNALS is not just technology; it helps you smoothen the way to a fast and MDR compliant market entry.
For Business Leaders and developers:
We look forward to discussing the concrete financial and operational advantages of using a pre-certified platform.
📍 VISIT US AT: Hall 12/SD19-13, Messe Düsseldorf
At our stand, we will highlight the immediate business value through:
API-First Platform in Action: A demonstration of how our API platform can serve as the backend for your medical application.
MDR IIa Certification Updates: How leveraging our certified services dramatically reduces regulatory risk and speeds up product launches.
HiBaby App Demonstration: A successful, real-world example of compliant, scalable patient monitoring (for maternal and infant care) built entirely on our platform.
Updated date:
Nov 11, 2025
