By 2022, the healthcare IoT will likely reach a valuation close to half of a trillion dollars. While many advancements push the connected healthcare market forward, ePHI (electronic protected health information) security remains a distinct challenge.
IoMT creates new pathways for knowledge sharing and analytics, but also opens the door to critical security challenges. Ransomware attacks in 2016 showed the world the vulnerabilities of healthcare organizations. The IoT-driven DDoS attack on Dyn Inc. only affected websites in late 2016. However, the next IoT-driven attack could render heart monitors or connected surgical tools unusable and put lives at risk. A vital factor in the future of data security is the understanding of both IoT and HIPAA compliance.
Current HIPAA regulations, specifically the Security Rule, discuss the accessibility, integrity, and confidentiality of all ePHI (electronic protected health information), but they don’t specifically govern IoT devices. All insurance companies, care providers, and clearinghouses that create, receive, use or maintain ePHI must protect any sensitive information.
For other entities, however, compliance isn’t as clear. Many unanswered questions highlight the need for additional legislation dictating who’s responsible for the protection of ePHI and IoT. For example, does an app/IoT device manufacturer owe consumers a HIPAA level of security for maintaining records of weight, heart rate, blood pressure, and other health insights?
In addition to the possibility of new covered entities, healthcare companies must consider the limitations of the HIPAA Security Rule. Like many cybersecurity standards, the rule only helps an organization provide reasonable care for ePHI. It does not outline case specifics for existing or new technologies.
The IoT industry may face additional regulations from the FDA, FCC, and the FTC among other entities, plus healthcare-specific regulations. In early 2015, the FTC released a report underscoring the need for security in the IoT industry. The Commission cited four main areas for consideration: data handling, consumer notification and choice, security, and the creation of formal legislation. Later this year in November 2017, a Drug Supply Chain Security Act (DSCSA) regulation will come into effect to track and trace medication, including serialization, reporting and verification tracking guidelines.
To protect themselves, IoT device manufacturers, software developers, and ePHI handlers can implement secure hardware and software measures according to industry best practices.
For instance, Apple recently revealed that they’re developing sensors to non invasively monitor blood sugar levels to treat diabetes. However, what they do with that data is critical; Apple’s health data will need to be stored in a secure, HIPAA-compliant data repository once it’s launched.
HIPAA may not yet address IoT devices specifically, but regulation and technology are inevitably connected. As industry standards evolve, use these best practices to protect patients and devices from dangerous attacks:
As the industry evolves and rules like HIPAA expand to govern IoT devices, take steps to protect your company from cyberthreats. HIPAA represents industry best practices that apply to all sensitive data.
Additional Resources on This Topic:
IoT Devices are Hackable in Under Three Minutes, Researchers Warn
New Healthcare IoT ideas on the Rise
Medical Internet of Things and Big Data in Healthcare
This article was first published on Onr.com
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