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The HIPAA Journal is the leading provider of HIPAA training, news, regulatory updates, and independent compliance advice.

Steve Alder

Steve Alder is the editor-in-chief of The HIPAA Journal. Steve is responsible for editorial policy regarding the topics covered in The HIPAA Journal. He is a specialist on healthcare industry legal and regulatory affairs, and has 10 years of experience writing about HIPAA and other related legal topics. Steve has developed a deep understanding of regulatory issues surrounding the use of information technology in the healthcare industry and has written hundreds of articles on HIPAA-related topics. Steve shapes the editorial policy of The HIPAA Journal, ensuring its comprehensive coverage of critical topics. Steve Alder is considered an authority in the healthcare industry on HIPAA. The HIPAA Journal has evolved into the leading independent authority on HIPAA under Steve’s editorial leadership. Steve manages a team of writers and is responsible for the factual and legal accuracy of all content published on The HIPAA Journal. Steve holds a Bachelor’s of Science degree from the University of Liverpool. You can connect with Steve via LinkedIn or email via stevealder(at)hipaajournal.com

Is Google Chat HIPAA Compliant?
Dec28

Is Google Chat HIPAA Compliant?

Google Chat is HIPAA compliant when it is used as part of a Google Workspace plan that includes the necessary controls to protect the confidentiality, integrity, and availability of Protected Health Information (PHI) used and disclosed via this communication channel. To make Google Chat HIPAA compliant, it is also necessary to agree to Google’s Business Associate Addendum to the Workspace Terms of Service. Google Chat is an intuitive messaging and team communication service that can be integrated with other services in the Google Workspace suite or third party workflow apps to enhance collaboration and workplace efficiency. Google Chat can also be used to communicate with external contacts subject to the permissions granted by system administrators and the controls put in place to prevent data loss. For organizations subject to the Health Insurance Portability and Accountability Act (HIPAA), these controls are necessary to support HIPAA compliance and prevent impermissible disclosures of PHI.  In addition, any HIPAA compliant service used to create, collect, store, or transmit PHI...

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Another Corewell Health Business Associate Suffers Million-Record Data Breach

The Michigan Attorney General’s Office announced on Tuesday that the protected health information of more than one million Corewell Health patients had been compromised in a cyberattack on one of Corewell Health’s vendors. HealthEC provides Corewell Health with a population health management platform that is used to identify high-risk patients in southeastern Michigan to close gaps in care and identify barriers to optimal care. HealthEC explained in its breach notification letters that suspicious activity was identified within its network and the forensic investigation determined that an unknown, unauthorized actor had access to some internal systems between July 14, 2023, and July 23, 2023. During that time, files containing protected health information were removed from its systems. HealthEC conducted a review of all files on the compromised part of the network and notified its affected clients on October 26, 2023. HealthEC then worked with those clients to issue notifications. According to the notification sent to the Maine Attorney General, HealthEC started mailing notification...

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HHS OIG Work Plan
Dec27

HHS OIG Work Plan

The HHS OIG Work Plan is a schedule of audits and evaluations conducted by the HHS Office of Inspector General that are intended to protect the integrity of HHS programs and the welfare of program beneficiaries. Unlike OIG Work Plans maintained by OIGs in other US Federal Government Departments, the HHS OIG Work Plan is “dynamic” and changes frequently to respond to emerging issues. The Role of the HHS OIG The role of the HHS OIG is to fight waste, fraud, and abuse in more than 100 HHS programs run by agencies such as the Centers for Medicare and Medicaid Services (CMS), the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA). It attempts to fulfil its role by conducting audits, evaluations, and – when necessary – investigations, and by providing outreach, compliance, and educational activities. Because OIG staff cannot be in all places at all times, HHS OIG schedules audits and evaluations based on mandatory review requirements, requests made by Congress, and reported management or performance issues. The HHS OIG Work Plan can be –...

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Seattle Children’s Hospital Sues Texas AG Over Demand for Trans Youth Medical Records

The Texas Attorney General sent a civil investigative demand to Seattle Children’s Hospital seeking access to the medical records of trans patients. The hospital refused to provide the records and has filed a lawsuit that requests a Texas judge nullify the Attorney General’s demands. The American Medical Association and the American Academy of Pediatrics believe that gender-affirming care is medically necessary and, in some cases, can be a lifesaving treatment for transgender youth; however, 20 states have imposed bans or placed restrictions on gender-affirming care for minors, and dozens of bills are being considered in other states. Earlier this year, Texas was added to that list when SB 14 was signed into law by Texas Governor Greg Abbott. The law prohibits the provision of gender transition care to Texas residents under 18 years of age. In November 2023, Texas Attorney General Ken Paxton issued a civil investigative demand for the records of Texas residents who visited Seattle Children’s Hospital to receive gender-affirming care when under 18 years of age. In Washington, gender...

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GAO: FDA Should Update Medical Device Cybersecurity Agreement
Dec27

GAO: FDA Should Update Medical Device Cybersecurity Agreement

The Government Accountability Office (GAO) has recommended the Food and Drug Administration (FDA) update its formal medical device agreement with the Cybersecurity and Infrastructure Security Agency (CISA), as the agreement is now five years old. The Consolidated Appropriations Act of 2023 includes a provision for GAO to review cybersecurity in medical devices and the FDA has primary responsibility for the cybersecurity of medical devices such as heart monitors. The FDA collaborates with CISA on security guidance for medical device manufacturers, public alerts about current vulnerabilities, and more, and facilitates collaboration with other federal agencies. While data from the Department of Health and Human Services do not show that vulnerabilities in medical devices are commonly exploited by malicious cyber actors, vulnerabilities in medical devices are a cause of concern as they could be exploited to cause harm to patients or to gain access to the internal networks to which the devices connect. Unauthorized access could result in delays to critical patient care, access being...

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