SERVICES
Digital Health Services
At ClariMed, our Digital Health Services are built on a foundation of rigorous engineering, human-centric design, and stringent regulatory compliance. We partner with healthcare innovators to design, develop, and deploy impactful solutions—enhancing patient care, streamlining clinical workflows, and meeting global standards for safety and security.
We operate as an extension of your team, focusing on agile processes, transparent communication, and measurable outcomes. By integrating usability, robust engineering, cybersecurity, quality validation, and seamless connectivity, we help clients bring transformative healthcare products to market with confidence.
Partner with us to accelerate your digital health innovation and deliver safe, reliable, and clinically meaningful solutions for the future of healthcare.
SERVICES
Digital Health Services
At ClariMed, our Digital Health Services are built on a foundation of rigorous engineering, human-centric design, and stringent regulatory compliance. We partner with healthcare innovators to design, develop, and deploy impactful solutions—enhancing patient care, streamlining clinical workflows, and meeting global standards for safety and security.
We operate as an extension of your team, focusing on agile processes, transparent communication, and measurable outcomes. By integrating usability, robust engineering, cybersecurity, quality validation, and seamless connectivity, we help clients bring transformative healthcare products to market with confidence.
Partner with us to accelerate your digital health innovation and deliver safe, reliable, and clinically meaningful solutions for the future of healthcare.
SERVICES
Digital Health Services
At ClariMed, our Digital Health Services are built on a foundation of rigorous engineering, human-centric design, and stringent regulatory compliance. We partner with healthcare innovators to design, develop, and deploy impactful solutions—enhancing patient care, streamlining clinical workflows, and meeting global standards for safety and security.
We operate as an extension of your team, focusing on agile processes, transparent communication, and measurable outcomes. By integrating usability, robust engineering, cybersecurity, quality validation, and seamless connectivity, we help clients bring transformative healthcare products to market with confidence.
Partner with us to accelerate your digital health innovation and deliver safe, reliable, and clinically meaningful solutions for the future of healthcare.
UX/UI Design
Effective UX/UI design is critical in medical devices, as it directly impacts patient safety, clinician efficiency, and overall user satisfaction. Poorly designed interfaces can lead to user errors, delays in critical care, and reduced adoption, making intuitive and accessible designs essential.
We design intuitive user experiences, transforming complex workflows into seamless interactions for clinicians, patients, and caregivers. With multi-language support, cultural localization, and compliance with IEC 62366, our interfaces enhance usability, safety, and engagement.
Human-Centered Design
Creating intuitive and accessible interfaces that cater to diverse user groups.
Iterative Prototyping
Developing prototypes for usability testing and incorporating real-time feedback.
Localization and Cultural Adaptation
Customizing interfaces for different languages and cultural contexts to ensure global usability.
Compliance with IEC 62366
Adhering to international standards for usability engineering in medical devices.
Visual Design Excellence
Crafting aesthetically pleasing interfaces to enhance user satisfaction and engagement.
Accessibility Considerations
Designing inclusive interfaces for users with varying abilities.
UX/UI Design
Effective UX/UI design is critical in medical devices, as it directly impacts patient safety, clinician efficiency, and overall user satisfaction. Poorly designed interfaces can lead to user errors, delays in critical care, and reduced adoption, making intuitive and accessible designs essential.
We design intuitive user experiences, transforming complex workflows into seamless interactions for clinicians, patients, and caregivers. With multi-language support, cultural localization, and compliance with IEC 62366, our interfaces enhance usability, safety, and engagement.
Human-Centered Design
Creating intuitive and accessible interfaces that cater to diverse user groups.
Iterative Prototyping
Developing prototypes for usability testing and incorporating real-time feedback.
Localization and Cultural Adaptation
Customizing interfaces for different languages and cultural contexts to ensure global usability.
Compliance with IEC 62366
Adhering to international standards for usability engineering in medical devices.
Visual Design Excellence
Crafting aesthetically pleasing interfaces to enhance user satisfaction and engagement.
Accessibility Considerations
Designing inclusive interfaces for users with varying abilities.
UX/UI Design
Effective UX/UI design is critical in medical devices, as it directly impacts patient safety, clinician efficiency, and overall user satisfaction. Poorly designed interfaces can lead to user errors, delays in critical care, and reduced adoption, making intuitive and accessible designs essential.
We design intuitive user experiences, transforming complex workflows into seamless interactions for clinicians, patients, and caregivers. With multi-language support, cultural localization, and compliance with IEC 62366, our interfaces enhance usability, safety, and engagement.
Human-Centered Design
Creating intuitive and accessible interfaces that cater to diverse user groups.
Iterative Prototyping
Developing prototypes for usability testing and incorporating real-time feedback.
Localization and Cultural Adaptation
Customizing interfaces for different languages and cultural contexts to ensure global usability.
Compliance with IEC 62366
Adhering to international standards for usability engineering in medical devices.
Visual Design Excellence
Crafting aesthetically pleasing interfaces to enhance user satisfaction and engagement.
Accessibility Considerations
Designing inclusive interfaces for users with varying abilities.
Software Development & Engineering
High-quality software is at the heart of innovation in medical devices, medtech, and pharmaceutical solutions. Our bespoke development services are purpose-built to meet the unique challenges of healthcare technology, ensuring seamless functionality, compliance, security, and scalability. Whether it’s Software in a Medical Device (SiMD) or Software as a Medical Device (SaMD), we deliver tailored solutions that prioritize safety, usability, and performance.
We adhere to both FDA guidance and international standards such as IEC 62304, ensuring compliance across all risk classifications. Our development processes are designed to meet the stringent requirements of medical devices, from Class A to Class C, while integrating robust cybersecurity measures to protect patient data and device functionality throughout the lifecycle. Our Full-Stack engineering expertise include:
Embedded Systems
We develop robust embedded software that powers the core functionality of medical devices. From RTOS and firmware engineering to hardware integration and connectivity protocols, our solutions deliver precision, reliability, and compliance with IEC 62304 across all risk classifications.
Desktop Applications
We create secure, user-friendly desktop applications designed for clinical environments, enhancing workflow efficiency and ensuring compliance with healthcare standards. These solutions seamlessly integrate with medical devices and healthcare systems, supporting critical decision-making.
Mobile Applications
Our mobile apps are tailored for patient engagement and clinical accessibility, providing intuitive, user-centric interfaces. From remote monitoring to real-time data sharing, we ensure seamless connectivity with devices and platforms.
Cloud and Web Solutions
We design scalable cloud and web platforms that enable secure device-to-cloud communication, advanced analytics, and remote care management. These solutions support real-time data sharing, interoperability, and compliance with FDA guidance and global security standards.
Software as a Medical Device (SaMD)
We specialize in standalone software solutions that perform critical medical functions, ensuring compliance with FDA guidance and IEC 62304. These SaMD solutions are tailored for diagnostics, patient monitoring, and therapeutic applications.
Software in a Medical Device (SiMD)
Our SiMD expertise integrates advanced software into medical devices, enhancing performance, functionality, and clinical outcomes. We ensure these embedded solutions meet stringent regulatory and safety requirements.
Our Approach
Custom, Client-Focused Solutions: We tailor every project to our client’s specific needs, delivering software that is purpose-built for medical applications.
Integrated Cybersecurity Measures: Embedding security into every layer of software development, including real-time threat monitoring, risk analysis, and compliance with FDA guidance and global security standards.
Agile Development Methodologies: Utilizing iterative, rapid development cycles to ensure timely delivery of scalable, high-quality solutions.
Cross-Platform Compatibility: Ensuring software operates seamlessly across embedded systems, desktop, mobile, and cloud platforms.
Regulatory Compliance at Every Step: Aligning with FDA guidance, IEC 62304, and global security standards to deliver software that meets benchmarks for safety, usability, and performance.
Our domain expertise spans medical devices, medtech, and pharmaceutical solutions. With a deep understanding of healthcare regulations, robust cybersecurity integration, and an unwavering commitment to innovation, we deliver software that exceeds expectations—secure, reliable, and ready for the future of healthcare.
Software Development & Engineering
High-quality software is at the heart of innovation in medical devices, medtech, and pharmaceutical solutions. Our bespoke development services are purpose-built to meet the unique challenges of healthcare technology, ensuring seamless functionality, compliance, security, and scalability. Whether it’s Software in a Medical Device (SiMD) or Software as a Medical Device (SaMD), we deliver tailored solutions that prioritize safety, usability, and performance.
We adhere to both FDA guidance and international standards such as IEC 62304, ensuring compliance across all risk classifications. Our development processes are designed to meet the stringent requirements of medical devices, from Class A to Class C, while integrating robust cybersecurity measures to protect patient data and device functionality throughout the lifecycle. Our Full-Stack engineering expertise include:
Embedded Systems
We develop robust embedded software that powers the core functionality of medical devices. From RTOS and firmware engineering to hardware integration and connectivity protocols, our solutions deliver precision, reliability, and compliance with IEC 62304 across all risk classifications.
Desktop Applications
We create secure, user-friendly desktop applications designed for clinical environments, enhancing workflow efficiency and ensuring compliance with healthcare standards. These solutions seamlessly integrate with medical devices and healthcare systems, supporting critical decision-making.
Mobile Applications
Our mobile apps are tailored for patient engagement and clinical accessibility, providing intuitive, user-centric interfaces. From remote monitoring to real-time data sharing, we ensure seamless connectivity with devices and platforms.
Cloud and Web Solutions
We design scalable cloud and web platforms that enable secure device-to-cloud communication, advanced analytics, and remote care management. These solutions support real-time data sharing, interoperability, and compliance with FDA guidance and global security standards.
Software as a Medical Device (SaMD)
We specialize in standalone software solutions that perform critical medical functions, ensuring compliance with FDA guidance and IEC 62304. These SaMD solutions are tailored for diagnostics, patient monitoring, and therapeutic applications.
Software in a Medical Device (SiMD)
Our SiMD expertise integrates advanced software into medical devices, enhancing performance, functionality, and clinical outcomes. We ensure these embedded solutions meet stringent regulatory and safety requirements.
Our Approach
Custom, Client-Focused Solutions: We tailor every project to our client’s specific needs, delivering software that is purpose-built for medical applications.
Integrated Cybersecurity Measures: Embedding security into every layer of software development, including real-time threat monitoring, risk analysis, and compliance with FDA guidance and global security standards.
Agile Development Methodologies: Utilizing iterative, rapid development cycles to ensure timely delivery of scalable, high-quality solutions.
Cross-Platform Compatibility: Ensuring software operates seamlessly across embedded systems, desktop, mobile, and cloud platforms.
Regulatory Compliance at Every Step: Aligning with FDA guidance, IEC 62304, and global security standards to deliver software that meets benchmarks for safety, usability, and performance.
Our domain expertise spans medical devices, medtech, and pharmaceutical solutions. With a deep understanding of healthcare regulations, robust cybersecurity integration, and an unwavering commitment to innovation, we deliver software that exceeds expectations—secure, reliable, and ready for the future of healthcare.
Software Development & Engineering
High-quality software is at the heart of innovation in medical devices, medtech, and pharmaceutical solutions. Our bespoke development services are purpose-built to meet the unique challenges of healthcare technology, ensuring seamless functionality, compliance, security, and scalability. Whether it’s Software in a Medical Device (SiMD) or Software as a Medical Device (SaMD), we deliver tailored solutions that prioritize safety, usability, and performance.
We adhere to both FDA guidance and international standards such as IEC 62304, ensuring compliance across all risk classifications. Our development processes are designed to meet the stringent requirements of medical devices, from Class A to Class C, while integrating robust cybersecurity measures to protect patient data and device functionality throughout the lifecycle. Our Full-Stack engineering expertise include:
Embedded Systems
We develop robust embedded software that powers the core functionality of medical devices. From RTOS and firmware engineering to hardware integration and connectivity protocols, our solutions deliver precision, reliability, and compliance with IEC 62304 across all risk classifications.
Desktop Applications
We create secure, user-friendly desktop applications designed for clinical environments, enhancing workflow efficiency and ensuring compliance with healthcare standards. These solutions seamlessly integrate with medical devices and healthcare systems, supporting critical decision-making.
Mobile Applications
Our mobile apps are tailored for patient engagement and clinical accessibility, providing intuitive, user-centric interfaces. From remote monitoring to real-time data sharing, we ensure seamless connectivity with devices and platforms.
Cloud and Web Solutions
We design scalable cloud and web platforms that enable secure device-to-cloud communication, advanced analytics, and remote care management. These solutions support real-time data sharing, interoperability, and compliance with FDA guidance and global security standards.
Software as a Medical Device (SaMD)
We specialize in standalone software solutions that perform critical medical functions, ensuring compliance with FDA guidance and IEC 62304. These SaMD solutions are tailored for diagnostics, patient monitoring, and therapeutic applications.
Software in a Medical Device (SiMD)
Our SiMD expertise integrates advanced software into medical devices, enhancing performance, functionality, and clinical outcomes. We ensure these embedded solutions meet stringent regulatory and safety requirements.
Our Approach
Custom, Client-Focused Solutions: We tailor every project to our client’s specific needs, delivering software that is purpose-built for medical applications.
Integrated Cybersecurity Measures: Embedding security into every layer of software development, including real-time threat monitoring, risk analysis, and compliance with FDA guidance and global security standards.
Agile Development Methodologies: Utilizing iterative, rapid development cycles to ensure timely delivery of scalable, high-quality solutions.
Cross-Platform Compatibility: Ensuring software operates seamlessly across embedded systems, desktop, mobile, and cloud platforms.
Regulatory Compliance at Every Step: Aligning with FDA guidance, IEC 62304, and global security standards to deliver software that meets benchmarks for safety, usability, and performance.
Our domain expertise spans medical devices, medtech, and pharmaceutical solutions. With a deep understanding of healthcare regulations, robust cybersecurity integration, and an unwavering commitment to innovation, we deliver software that exceeds expectations—secure, reliable, and ready for the future of healthcare.
Cybersecurity Solutions
In today’s interconnected healthcare landscape, safeguarding medical devices against cyber threats is critical to ensuring patient safety, regulatory compliance, and device reliability. Cybersecurity is a top priority for regulatory agencies, with the FDA consistently emphasizing its importance during the review process. Addressing vulnerabilities is essential not only for achieving regulatory approval but also for maintaining trust in your products and protecting patient data.
At ClariMed, we bring deep expertise in medical device cybersecurity, delivering comprehensive solutions tailored to the evolving needs of healthcare technology. From development to deployment—and beyond—we embed cybersecurity into every layer of your software, ensuring resilience against evolving threats and compliance with FDA guidance and global standards.
Threat Modeling and Risk Assessment
Identifying vulnerabilities during the design phase to develop proactive mitigation strategies and align with FDA expectations and international standards.
Cybersecurity Risk Assessments
Providing detailed evaluations of your device’s security posture to ensure compliance with IEC 62304 and FDA guidance.
Secure Software Development Lifecycle (SDLC)
Embedding security best practices into every phase of software development to ensure resilience against evolving threats.
Post-Market Cybersecurity Management
Offering strategies for maintaining device security post-launch, including secure updates, monitoring, and vulnerability management.
Data Encryption and Protection
Ensuring the confidentiality and integrity of patient data through advanced encryption methods for storage and transmission.
Authentication and Access Control
Implementing robust mechanisms to restrict unauthorized access and ensure user accountability.
Why Choose ClariMed?
Cybersecurity is at the core of ClariMed’s commitment to innovation and safety. Our team combines deep expertise in medtech and regulatory compliance with a proactive approach to addressing evolving cyber threats.
Regulatory Expertise: We have extensive experience navigating FDA reviews and ensuring compliance with global cybersecurity requirements.
Integrated Lifecycle Solutions: Our cybersecurity measures are embedded at every stage of development, deployment, and post-market management to ensure comprehensive protection.
Tailored Services: Every solution is bespoke, designed to address the unique cybersecurity challenges of your device or platform.
Whether through detailed threat modeling, risk assessments, or secure software development, we deliver solutions that inspire confidence and protect your devices, patients, and data.
Cybersecurity Solutions
In today’s interconnected healthcare landscape, safeguarding medical devices against cyber threats is critical to ensuring patient safety, regulatory compliance, and device reliability. Cybersecurity is a top priority for regulatory agencies, with the FDA consistently emphasizing its importance during the review process. Addressing vulnerabilities is essential not only for achieving regulatory approval but also for maintaining trust in your products and protecting patient data.
At ClariMed, we bring deep expertise in medical device cybersecurity, delivering comprehensive solutions tailored to the evolving needs of healthcare technology. From development to deployment—and beyond—we embed cybersecurity into every layer of your software, ensuring resilience against evolving threats and compliance with FDA guidance and global standards.
Threat Modeling and Risk Assessment
Identifying vulnerabilities during the design phase to develop proactive mitigation strategies and align with FDA expectations and international standards.
Cybersecurity Risk Assessments
Providing detailed evaluations of your device’s security posture to ensure compliance with IEC 62304 and FDA guidance.
Secure Software Development Lifecycle (SDLC)
Embedding security best practices into every phase of software development to ensure resilience against evolving threats.
Post-Market Cybersecurity Management
Offering strategies for maintaining device security post-launch, including secure updates, monitoring, and vulnerability management.
Data Encryption and Protection
Ensuring the confidentiality and integrity of patient data through advanced encryption methods for storage and transmission.
Authentication and Access Control
Implementing robust mechanisms to restrict unauthorized access and ensure user accountability.
Why Choose ClariMed?
Cybersecurity is at the core of ClariMed’s commitment to innovation and safety. Our team combines deep expertise in medtech and regulatory compliance with a proactive approach to addressing evolving cyber threats.
Regulatory Expertise: We have extensive experience navigating FDA reviews and ensuring compliance with global cybersecurity requirements.
Integrated Lifecycle Solutions: Our cybersecurity measures are embedded at every stage of development, deployment, and post-market management to ensure comprehensive protection.
Tailored Services: Every solution is bespoke, designed to address the unique cybersecurity challenges of your device or platform.
Whether through detailed threat modeling, risk assessments, or secure software development, we deliver solutions that inspire confidence and protect your devices, patients, and data.
Cybersecurity Solutions
In today’s interconnected healthcare landscape, safeguarding medical devices against cyber threats is critical to ensuring patient safety, regulatory compliance, and device reliability. Cybersecurity is a top priority for regulatory agencies, with the FDA consistently emphasizing its importance during the review process. Addressing vulnerabilities is essential not only for achieving regulatory approval but also for maintaining trust in your products and protecting patient data.
At ClariMed, we bring deep expertise in medical device cybersecurity, delivering comprehensive solutions tailored to the evolving needs of healthcare technology. From development to deployment—and beyond—we embed cybersecurity into every layer of your software, ensuring resilience against evolving threats and compliance with FDA guidance and global standards.
Threat Modeling and Risk Assessment
Identifying vulnerabilities during the design phase to develop proactive mitigation strategies and align with FDA expectations and international standards.
Cybersecurity Risk Assessments
Providing detailed evaluations of your device’s security posture to ensure compliance with IEC 62304 and FDA guidance.
Secure Software Development Lifecycle (SDLC)
Embedding security best practices into every phase of software development to ensure resilience against evolving threats.
Post-Market Cybersecurity Management
Offering strategies for maintaining device security post-launch, including secure updates, monitoring, and vulnerability management.
Data Encryption and Protection
Ensuring the confidentiality and integrity of patient data through advanced encryption methods for storage and transmission.
Authentication and Access Control
Implementing robust mechanisms to restrict unauthorized access and ensure user accountability.
Why Choose ClariMed?
Cybersecurity is at the core of ClariMed’s commitment to innovation and safety. Our team combines deep expertise in medtech and regulatory compliance with a proactive approach to addressing evolving cyber threats.
Regulatory Expertise: We have extensive experience navigating FDA reviews and ensuring compliance with global cybersecurity requirements.
Integrated Lifecycle Solutions: Our cybersecurity measures are embedded at every stage of development, deployment, and post-market management to ensure comprehensive protection.
Tailored Services: Every solution is bespoke, designed to address the unique cybersecurity challenges of your device or platform.
Whether through detailed threat modeling, risk assessments, or secure software development, we deliver solutions that inspire confidence and protect your devices, patients, and data.
Software Quality & Validation
Ensuring the quality and reliability of software in medical devices is a critical component of patient safety and regulatory compliance. With stringent requirements from agencies like the FDA and standards such as IEC 62304, the validation process is essential to building trust in your product and achieving market success. At ClariMed, we specialize in providing comprehensive quality and validation services that meet the highest regulatory standards and ensure the seamless functionality of your software.
Comprehensive Quality Engineering
Robust processes ensure every stage of software development adheres to rigorous quality standards, from requirements gathering to deployment.
Verification and Validation (V&V) 2
Comprehensive testing protocols, including automated, unit, integration, and system-level testing, confirm product functionality, reliability, and compliance with regulatory expectations.
Compliance and Technical Assessment Services
Software Quality Compliance Assessment: Evaluating your software lifecycle processes to ensure alignment with FDA guidance and IEC 62304, while providing actionable recommendations for improvement.
Technical Assessment: Detailed analysis of software architecture, design, and code to uncover opportunities for optimization and enhanced maintainability.
Your Partner in Quality and Compliance
At ClariMed, we go beyond basic quality assurance to act as your trusted partner in navigating the complexities of regulatory landscapes. With extensive experience aligning with FDA guidance and IEC 62304, we simplify compliance and reduce time-to-market delays.
We provide end-to-end traceability of requirements, design, and testing to ensure full transparency during regulatory submissions.
Our actionable insights and tailored assessments streamline submission preparation, ensuring confidence throughout the review process.
By integrating risk-based validation and robust documentation practices, we empower you to meet global compliance demands with ease.
Let ClariMed help you deliver innovative, reliable medical device software that inspires confidence, achieves regulatory approval, and improves patient outcomes.
Software Quality & Validation
Ensuring the quality and reliability of software in medical devices is a critical component of patient safety and regulatory compliance. With stringent requirements from agencies like the FDA and standards such as IEC 62304, the validation process is essential to building trust in your product and achieving market success. At ClariMed, we specialize in providing comprehensive quality and validation services that meet the highest regulatory standards and ensure the seamless functionality of your software.
Comprehensive Quality Engineering
Robust processes ensure every stage of software development adheres to rigorous quality standards, from requirements gathering to deployment.
Verification and Validation (V&V) 2
Comprehensive testing protocols, including automated, unit, integration, and system-level testing, confirm product functionality, reliability, and compliance with regulatory expectations.
Compliance and Technical Assessment Services
Software Quality Compliance Assessment: Evaluating your software lifecycle processes to ensure alignment with FDA guidance and IEC 62304, while providing actionable recommendations for improvement.
Technical Assessment: Detailed analysis of software architecture, design, and code to uncover opportunities for optimization and enhanced maintainability.
Your Partner in Quality and Compliance
At ClariMed, we go beyond basic quality assurance to act as your trusted partner in navigating the complexities of regulatory landscapes. With extensive experience aligning with FDA guidance and IEC 62304, we simplify compliance and reduce time-to-market delays.
We provide end-to-end traceability of requirements, design, and testing to ensure full transparency during regulatory submissions.
Our actionable insights and tailored assessments streamline submission preparation, ensuring confidence throughout the review process.
By integrating risk-based validation and robust documentation practices, we empower you to meet global compliance demands with ease.
Let ClariMed help you deliver innovative, reliable medical device software that inspires confidence, achieves regulatory approval, and improves patient outcomes.
Software Quality & Validation
Ensuring the quality and reliability of software in medical devices is a critical component of patient safety and regulatory compliance. With stringent requirements from agencies like the FDA and standards such as IEC 62304, the validation process is essential to building trust in your product and achieving market success. At ClariMed, we specialize in providing comprehensive quality and validation services that meet the highest regulatory standards and ensure the seamless functionality of your software.
Comprehensive Quality Engineering
Robust processes ensure every stage of software development adheres to rigorous quality standards, from requirements gathering to deployment.
Verification and Validation (V&V) 2
Comprehensive testing protocols, including automated, unit, integration, and system-level testing, confirm product functionality, reliability, and compliance with regulatory expectations.
Compliance and Technical Assessment Services
Software Quality Compliance Assessment: Evaluating your software lifecycle processes to ensure alignment with FDA guidance and IEC 62304, while providing actionable recommendations for improvement.
Technical Assessment: Detailed analysis of software architecture, design, and code to uncover opportunities for optimization and enhanced maintainability.
Your Partner in Quality and Compliance
At ClariMed, we go beyond basic quality assurance to act as your trusted partner in navigating the complexities of regulatory landscapes. With extensive experience aligning with FDA guidance and IEC 62304, we simplify compliance and reduce time-to-market delays.
We provide end-to-end traceability of requirements, design, and testing to ensure full transparency during regulatory submissions.
Our actionable insights and tailored assessments streamline submission preparation, ensuring confidence throughout the review process.
By integrating risk-based validation and robust documentation practices, we empower you to meet global compliance demands with ease.
Let ClariMed help you deliver innovative, reliable medical device software that inspires confidence, achieves regulatory approval, and improves patient outcomes.
Connectivity and Interoperability
Seamlessly connecting medical devices to the broader digital ecosystem is essential for advancing healthcare technology and improving workflows. At ClariMed, we specialize in delivering comprehensive connectivity and interoperability solutions, designed to meet the unique needs of medical devices while adhering to the highest standards of security and compliance. We provide custom solutions that bridge the gap between devices, systems, and platforms, enabling secure, real-time communication and seamless integration:
Device-to-Cloud Communication
Enabling secure, real-time connectivity between devices and cloud platforms for remote monitoring, diagnostics, firmware updates, and performance tracking.
EHR/LIS/ELN Integration
Developing solutions that ensure seamless interoperability with electronic health records (EHR), laboratory information systems (LIS), and electronic lab notebooks (ELN), leveraging standards like HL7 and FHIR for efficient data exchange.
Custom Data Connectivity Solutions
Creating tools that enable clients to collect and transfer data from devices for research, development, or other internal needs. These solutions integrate seamlessly into existing systems or workflows.
Companion Application Development
Designing auxiliary applications that enhance device functionality, improve user engagement, and support secure data visualization tailored to your unique needs.
Scalable Cloud Solutions
Building robust, cloud-based infrastructures for device connectivity, enabling smooth data flow, system integration, and growth with your evolving needs.
Why Choose ClariMed?
ClariMed delivers bespoke connectivity solutions tailored to your device’s unique needs. Our expertise in device integration, secure data flow, and regulatory compliance ensures seamless interoperability across platforms. With a commitment to quality and innovation, we help you bridge the gap between medical devices and the digital healthcare ecosystem.
Connectivity and Interoperability
Seamlessly connecting medical devices to the broader digital ecosystem is essential for advancing healthcare technology and improving workflows. At ClariMed, we specialize in delivering comprehensive connectivity and interoperability solutions, designed to meet the unique needs of medical devices while adhering to the highest standards of security and compliance. We provide custom solutions that bridge the gap between devices, systems, and platforms, enabling secure, real-time communication and seamless integration:
Device-to-Cloud Communication
Enabling secure, real-time connectivity between devices and cloud platforms for remote monitoring, diagnostics, firmware updates, and performance tracking.
EHR/LIS/ELN Integration
Developing solutions that ensure seamless interoperability with electronic health records (EHR), laboratory information systems (LIS), and electronic lab notebooks (ELN), leveraging standards like HL7 and FHIR for efficient data exchange.
Custom Data Connectivity Solutions
Creating tools that enable clients to collect and transfer data from devices for research, development, or other internal needs. These solutions integrate seamlessly into existing systems or workflows.
Companion Application Development
Designing auxiliary applications that enhance device functionality, improve user engagement, and support secure data visualization tailored to your unique needs.
Scalable Cloud Solutions
Building robust, cloud-based infrastructures for device connectivity, enabling smooth data flow, system integration, and growth with your evolving needs.
Why Choose ClariMed?
ClariMed delivers bespoke connectivity solutions tailored to your device’s unique needs. Our expertise in device integration, secure data flow, and regulatory compliance ensures seamless interoperability across platforms. With a commitment to quality and innovation, we help you bridge the gap between medical devices and the digital healthcare ecosystem.
Connectivity and Interoperability
Seamlessly connecting medical devices to the broader digital ecosystem is essential for advancing healthcare technology and improving workflows. At ClariMed, we specialize in delivering comprehensive connectivity and interoperability solutions, designed to meet the unique needs of medical devices while adhering to the highest standards of security and compliance. We provide custom solutions that bridge the gap between devices, systems, and platforms, enabling secure, real-time communication and seamless integration:
Device-to-Cloud Communication
Enabling secure, real-time connectivity between devices and cloud platforms for remote monitoring, diagnostics, firmware updates, and performance tracking.
EHR/LIS/ELN Integration
Developing solutions that ensure seamless interoperability with electronic health records (EHR), laboratory information systems (LIS), and electronic lab notebooks (ELN), leveraging standards like HL7 and FHIR for efficient data exchange.
Custom Data Connectivity Solutions
Creating tools that enable clients to collect and transfer data from devices for research, development, or other internal needs. These solutions integrate seamlessly into existing systems or workflows.
Companion Application Development
Designing auxiliary applications that enhance device functionality, improve user engagement, and support secure data visualization tailored to your unique needs.
Scalable Cloud Solutions
Building robust, cloud-based infrastructures for device connectivity, enabling smooth data flow, system integration, and growth with your evolving needs.
Why Choose ClariMed?
ClariMed delivers bespoke connectivity solutions tailored to your device’s unique needs. Our expertise in device integration, secure data flow, and regulatory compliance ensures seamless interoperability across platforms. With a commitment to quality and innovation, we help you bridge the gap between medical devices and the digital healthcare ecosystem.
Let's work together!
Contact us to discuss how we can advance your medical device development efforts together.
Let's work together!
Contact us to discuss how we can advance your medical device development efforts together.
Let's work together!
Contact us to discuss how we can advance your medical device development efforts together.