Medical Device Cybersecurity Assessment
Guaranteeing Secure Healthcare Technology
With 20 years in cybersecurity and 18 years in healthcare IT, ScienceSoft helps evaluate and improve the security of medical devices, SaMD, and medical device networks at any stage of their lifecycle.
Medical device cybersecurity assessment helps medical device manufacturers reveal any security gaps in their products before they go on the market, ensuring their safety in the long run, also as a part of the postmarket management strategy. For healthcare providers, it is a way to verify that the medical devices they employ don’t contain vulnerabilities that could compromise healthcare operations, patient safety, or sensitive data privacy.
Medical Devices and Software We Assess
ScienceSoft finds and helps remediate security issues in connected medical devices as well as software as a medical device (SaMD). This includes:
Class II Medical Devices
- Medical imaging devices: e.g., ultrasound, MRI, and CT scanners.
- Monitoring and diagnostic devices: e.g., wearable spirometers, hemodynamic/pressure monitoring devices, ECG patches.
- Treatment devices: e.g., anesthesia machines, insulin pumps, smart insulin pens, hemodialysis machines, smart intravenous infusion pumps.
Class III Medical Devices
- Implants: e.g., pacemakers, cardioverter-defibrillators, cochlear implants, neural prostheses.
- Emergency and intensive care devices: e.g., cardiac ablation systems, high frequency ventilators.
- Critical obstetric electronic devices: e.g., obstetric data analyzers, fetal EEG monitors.
SaMD (Class I, II, III)
- Software for monitoring and diagnostics: e.g., image recognition software for stroke type identification or cancer tumor localization.
- Software for treatment and disease management: e.g., medication dosing calculators, apps for identification of sleep apnea episodes, AI-driven solutions for disease treatment and patient care planning.
Security Assessment Approaches We Are Confident In
We review the existing security controls to determine which ones are lacking:
- Medical device hardware and software features that protect critical functionality and data.
- Secure software architecture.
- Secure development life cycle.
- Patching schedule.
- Infrastructure configuration (including cloud).
- Device security monitoring, response and recovery policy.
- Security tools employed, their configuration and integrations.
- Security awareness of the device users and healthcare workers who interact with the device.
To identify all security vulnerabilities that can potentially endanger medical device data or functionality, we:
- Scan the device and its infrastructure, including within a broad system (e.g., IoT) if needed.
- Manually analyze the scanning results to exclude false positives.
- Analyze and prioritize the detected vulnerabilities to offer the optimal remediation roadmap.
Acting like real-world hackers, we try to exploit the existing vulnerabilities to see if malicious actors can break into the system. We perform penetration tests according to the three main offender models:
- Black box. We approach the medical device/ system without any prior knowledge of it. We search for publicly available info about the device, its manufacturer, or end users, which we can use in attack simulation.
- Gray box. We have limited info about the device or its use environment: e.g., the device user credentials, low-privileged access to a hospital network where the device is placed.
- White box. We receive admin access and full information about the architecture and tech stack of the tested device to review its source code.
To test the security awareness of the device users (for healthcare providers) or employees (for device manufacturers), we can simulate:
- Phishing attacks – malicious emails sent to multiple users to test their security vigilance and the efficiency of email filtering.
- Spear phishing – emails targeting specific employees (e.g., admins) to trick them into giving access to the device to an unauthorized user or a user having a lower access level.
- Whaling – emails targeting C-level executives.
To evaluate and mitigate the risks that affect your medical device, we:
- Identify cybersecurity gaps in the device and the IT infrastructure it is a part of.
- Define the security threats posed by the vulnerabilities: data breaches, malware spread, modifying device operation algorithms, etc.
- Assess the likelihood of vulnerability exploitation and the severity of its potential consequences: e.g., sensitive data exposure, compliance breaches, harm to patients’ health, damage to the IT infrastructure.
- Classify the risks according to their control level.
- Offer actionable risk mitigation guidance.
ScienceSoft Is a Leader in Healthcare IT Services Market in 2022 SPARK Matrix
ScienceSoft is featured as a leading healthcare IT services provider, along with Athena Health and Oracle Cerner. This achievement is a result of 18 years of tireless pursuit of technological innovation, made possible by ScienceSoft’s passionate team of healthcare IT experts who always strive to make a difference for patients and caregivers alike.
Deliverables You Get Upon Medical Device Cybersecurity Assessment
For devices at any stage of their lifecycle
- Security audit reports.
- Vulnerability assessment reports.
- Penetration testing reports.
- Summary of the risk assessment conclusions, including the control level of the revealed risks.
In these reports, we include:
- A summary of the detected flaws, vulnerabilities, risks, compliance gaps.
- Remediation guidelines.
For device premarket submission
To help ensure continuous safety and effectiveness of a medical device, we offer:
- A detailed description of the security controls in place to ensure that the device will maintain its integrity from the point of origin to the point where it leaves the control of the manufacturer.
- A plan for security updates and patches throughout the medical device lifecycle.
- Guidelines on the cybersecurity controls for the intended use environment (e.g., how to place and configure security tools such as antivirus software, firewalls, SIEM).
For devices on the market
If vulnerability remediation resulted in changes to the device software, they need to be reported to FDA or a Notified Body designated under MDR/IVDR. In this case, we provide:
- Detailed description of the vulnerability and the changes made to the device, including the comparison between the current and the previously approved version of it.
- The rationale for making the changes.
- References to other devices that were modified in response to the same vulnerability.
Prof. Dr. Department of Biomedical Science
During our cooperation, ScienceSoft proved to have vast expertise in the Healthcare and Life Science industries related to the development of desktop software connected to laboratory equipment, a mobile application, and a data analytics platform. They bring top-quality talents and deep knowledge of IT technologies and approaches in accordance with ISO 13485 and IEC 62304 standards.
President & CEO
bioAffinity Technologies hired ScienceSoft to help in the development of its automated data analysis software for detection of lung cancer using flow cytometry. Our project required a large amount of industry specific methodology and algorithms to be implemented into our new software connected to EHR/LIS systems, which the team handled well. They are reliable, thorough, smart, available, extremely good communicators and very friendly.
ScienceSoft as a Responsible Healthcare Security Partner
Consistency in service quality
- Established quality management system for medical devices and SaMD confirmed by ISO 13485 certification.
- ISO 9001-certified to guarantee quality performance and timely project delivery.
- ISO 27001 certification ensuring full security of the sensitive data entrusted to us.
- A top HIPAA consulting company in 2022, according to Atlantic.net.
- Winner of Health Tech Digital Awards 2022 in the category Best Healthcare Technology Solution of the Year.
- Recognized as Top Penetration Testing Company by Clutch.
- For the second straight year, ScienceSoft USA Corporation is listed among The Americas’ Fastest-Growing Companies by the Financial Times.
Doubtful About Cybersecurity Assessment for Your Healthcare Device? Let Us Dispel Your Concerns
With so many regulations that may apply to one medical device — FDA, MDR/IVDR, HIPAA, GDPR — can you help prevent all possible compliance breaches?
As an ISO 13485-certified tech partner, we know how to meet the requirements of the FDA and the Council of the European Union. We have hands-on experience with HIPAA and GDPR compliance. Our team of regulatory consultants, security engineers, and healthcare software developers can evaluate, implement, or improve the administrative and technical safeguards as required by these regulations. We are also ready to guide you through HIPAA/GDPR risk assessment and FDA/CE/MDR/IVDR submission process.
A high-level security assessment of our medical device is not enough. Will we get actionable insights to promptly address the assessment findings?
Our security assessments are result-oriented and focused on providing valuable deliverables. The transparent documentation we create helps with market registration, becomes a part of the post-market vulnerability management strategy, and drives the necessary remediation activities.
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Development of a Secure Physiotherapy Platform for AKLOS Health
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Pentesting of a Web Platform and Mobile Apps for a Remote Patient Monitoring Vendor
ScienceSoft conducted gray box penetration testing of a remote patient monitoring platform and corresponding mobile iOS and Android apps to help ensure PHI protection in line with HITRUST CSF and HIPAA.
Network Pentesting and a Phishing Campaign for a US Healthcare Provider
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Development of a Secure Brain Tumor Localization Application
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Penetration Testing of the Hospital IT Infrastructure for a US Health System
To safeguard a hospital’s complex IT infrastructure against vulnerabilities that could disrupt healthcare procedures or lead to HIPAA compliance breaches, ScienceSoft conducted gray box penetration testing and provided exhaustive remediation guidance.