Text of VT S 173 (2024)
An act relating to the collection, sharing, and selling of consumer health data
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As introduced
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S.173
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Introduced by Senator Lyons
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Referred to Committee on
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Date:
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Subject: Health; health information; data privacy
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Statement of purpose of bill as introduced: This bill proposes to regulate the
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collection, sharing, and selling of consumer health data in Vermont.
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An act relating to the collection, sharing, and selling of consumer health
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data
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It is hereby enacted by the General Assembly of the State of Vermont:
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Sec. 1. 18 V.S.A. chapter 42B is amended to read:
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42B. HEALTH CARE PRIVACY
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Subchapter 1. Disclosure of Protected Health Information
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§ 1881. DISCLOSURE OF PROTECTED HEALTH INFORMATION
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PROHIBITED
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* * *
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Subchapter 2. Vermont My Health My Data Act
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§ 1891. SHORT TITLE
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This subchapter shall be known and may be cited as the “Vermont My
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Health My Data Act.”
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§ 1892. FINDINGS AND INTENT
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(a) Findings. The General Assembly finds that:
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(1) The residents of Vermont regard their privacy as a fundamental right
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and an essential element of their individual freedom. Fundamental privacy
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rights have long been and continue to be integral to protecting Vermonters and
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to safeguarding our democratic republic.
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(2) Information related to an individual’s health conditions or attempts
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to obtain health care services is among the most personal and sensitive
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categories of data collected. Vermonters expect that their health data is
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protected under laws like the Health Insurance Portability and Accountability
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Act of 1996 (HIPAA). However, HIPAA only covers health data collected by
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specific health care entities, including most health care providers. Health data
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collected by noncovered entities, including certain applications and websites,
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are not afforded the same protections. This act works to close the gap between
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consumer knowledge and industry practice by providing stronger privacy
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protections for all of Vermont consumers’ health data.
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(b) Intent. By enacting this act, it is the intent of the General Assembly to
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provide heightened protections for Vermonters’ health data by:
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(1) requiring additional disclosures and consumer consent regarding the
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collection, sharing, and use of their health data;
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(2) empowering consumers with the right to have their health data
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deleted;
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(3) prohibiting the selling of consumer health data without valid
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authorization signed by the consumer; and
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(4) making it unlawful to utilize a geofence around a facility that
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provides health care services.
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§ 1893. DEFINITIONS
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As used in this subchapter:
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(1) “Abortion” means any medical treatment intended to induce the
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termination of, or to terminate, a clinically diagnosable pregnancy except for
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the purpose of producing a live birth.
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(2) “Affiliate” means a legal entity that shares common branding with
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another legal entity and controls, is controlled by, or is under common control
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with another legal entity. For purposes of this definition, “control” or
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“controlled” means any one or more of the following:
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(A) ownership of, or the power to vote, more than 50 percent of the
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outstanding shares of any class of voting security of a company;
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(B) control in any manner over the election of a majority of the
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directors or of individuals exercising similar functions; or
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(C) the power to exercise controlling influence over the management
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of a company.
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(3) “Authenticate” means to use reasonable means to determine that a
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request to exercise any of the rights afforded in this chapter is being made by
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or on behalf of the consumer who is entitled to exercise those consumer rights
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with respect to the consumer health data at issue.
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(4) “Biometric data” means data that is generated from the measurement
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or technological processing of an individual’s physiological, biological, or
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behavioral characteristics and that identifies a consumer, whether individually
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or in combination with other data. Biometric data includes:
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(A) imagery of the iris, retina, fingerprint, face, hand, palm, vein
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patterns, and voice recordings, from which an identifier template can be
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extracted; and
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(B) keystroke patterns or rhythms and gait patterns or rhythms that
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contain identifying information.
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(5) “Collect” means to buy, rent, access, retain, receive, acquire, infer,
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derive, or otherwise process consumer health data in any manner.
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(6)(A) “Consent” means a clear affirmative act that signifies the
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consumer’s freely given, specific, informed, opt-in, voluntary, and
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unambiguous agreement, which may include written consent provided by
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electronic means.
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(B) “Consent” shall not be obtained by:
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(i) a consumer’s acceptance of a general or broad terms-of-use
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agreement or a similar document that contains descriptions of personal data
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processing along with other unrelated information;
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(ii) a consumer hovering over, muting, pausing, or closing a given
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piece of content; or
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(iii) a consumer’s agreement obtained through the use of deceptive
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designs.
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(7)(A) “Consumer” means a natural person who meets one or both of
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the following conditions:
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(i) the person is a Vermont resident; or
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(ii) the person’s consumer health data is collected in Vermont.
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(B) “Consumer” means a natural person who acts only in an
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individual or household context, however identified, including by any unique
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identifier. The term does not include an individual acting in an employment
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context.
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(8)(A) “Consumer health data” means personal information that is
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linked or reasonably linkable to a consumer and that identifies the consumer’s
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past, present, or future physical or mental health status.
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(B) For purposes of this definition, physical or mental health status
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includes:
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(i) individual health conditions, treatment diseases, or diagnosis;
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(ii) social, psychological, behavioral, and medical interventions;
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(iii) health-related surgeries or procedures;
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(iv) use or purchased of prescribed medication;
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(v) bodily functions, vital signs, symptoms, or measurements of
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the information described in this subdivision (B);
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(vi) diagnoses or diagnostic testing, treatment, or medication;
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(vii) gender-affirming care information;
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(viii) reproductive or sexual health information;
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(ix) biometric data;
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(x) genetic data;
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(xi) precise location information that could reasonably indicate a
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consumer’s attempt to acquire or receive health services or supplies;
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(xii) data that identifies a consumer seeking health care services;
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or
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(xiii) any information that a regulated entity or a small business,
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or its respective processor, processes to associate or identify a consumer with
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the data described in subdivisions (i)–(xii) of this subdivision (B) that is
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derived or extrapolated from nonhealth information, such as proxy, derivative,
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inferred, or emergency data by any means, including algorithms or machine
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learning.
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(C) “Consumer health data” does not include personal information
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that is used to engage in public or peer-reviewed scientific, historical, or
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statistical research in the public interest that adheres to all other applicable
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ethics and privacy laws and is approved, monitored, and governed by an
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institutional review board, human subjects research ethics review board, or a
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similar independent oversight entity that determines that the regulated entity or
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the small business has implemented reasonable safeguards to mitigate privacy
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risks associated with research, including any risks associated with
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reidentification.
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(9) “Deceptive design” means a user interface designed or manipulated
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with the effect of subverting or impairing user autonomy, decision making, or
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choice.
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(10) “Deidentified data” means data that cannot reasonably be used to
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infer information about, or otherwise be linked to, an identified or identifiable
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consumer, or a device linked to such consumer, if the regulated entity or the
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small business that possesses the data does all of the following:
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(A) takes reasonable measures to ensure that the data cannot be
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associated with a consumer;
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(B) publicly commits to process the data only in a deidentified
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fashion and not to attempt to reidentify the data; and
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(C) contractually obligates any recipients of the data to satisfy the
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criteria set forth in this subdivision (10).
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(11) “Gender-affirming care information” means personal information
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relating to seeking or obtaining past, present, or future gender-affirming health
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care services. “Gender-affirming care information” includes:
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(A) precise location information that could reasonably indicate a
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consumer’s attempt to acquire or receive gender-affirming health care services;
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(B) efforts to research or obtain gender-affirming health care
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services; or
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(C) any gender-affirming care information that is derived,
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extrapolated, or inferred, including from nonhealth information such as proxy,
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derivative, inferred, emergent, or algorithmic data.
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(12) “Gender-affirming health care services” has the same meaning as in
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1 V.S.A. § 150.
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(13) “Genetic data” means any data, regardless of its format, that
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concerns a consumer’s genetic characteristics. “Genetic data” includes:
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(A) raw sequence data that result from the sequencing of a
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consumer’s complete extracted deoxyribonucleic acid (DNA) or a portion of
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the extracted DNA;
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(B) genotypic and phenotypic information that results from analyzing
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the raw sequence data; and
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(C) self-reported health data that a consumer submits to a regulated
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entity or a small business and that is analyzed in connection with the
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consumer’s raw sequence data.
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(14) “Geofence” means technology that uses global positioning
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coordinates, cell tower connectivity, cellular data, radio frequency
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identification, Wi-Fi data, or any other form of spatial or location detection,
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individually or in combination, to establish a virtual boundary around a
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specific physical location or to locate a consumer within a virtual boundary.
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For purposes of this definition, “geofence” means a virtual boundary that is
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2,000 feet or less from the perimeter of the physical location.
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(15) “Health care service” means any service provided to a person to
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assess, measure, improve, or learn about a person’s mental or physical health,
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including:
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(A) individual health conditions, status, diseases, or diagnoses;
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(B) social, psychological, behavioral, and medical interventions;
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(C) health-related surgeries or procedures;
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(D) use or purchase of medication;
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(E) bodily functions, vital signs, symptoms, or measurements of the
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information described in this subdivision (15);
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(F) diagnoses or diagnostic testing, treatment, or medication;
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(G) reproductive health services; or
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(H) gender-affirming health care services.
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(16) “Homepage” means the introductory page of an internet website
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and any internet web page on which personal information is collected. In the
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case of an online service such as a mobile application, “homepage” means the
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application’s platform page or download page, and a link within the
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application, such as from the application configuration or the “about,”
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“information,” or “settings” page.
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(17) “Person” means, where applicable, a natural person, corporation,
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trust, unincorporated association, or partnership. The term does not include a
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government agency, tribal nation, or a contracted service provider when
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processing consumer health data on behalf of a government agency.
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(18)(A) “Personal information” means information that identifies or is
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reasonably capable of being associated or linked, directly or indirectly, with a
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particular consumer. “Personal information” includes data associated with a
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persistent unique identifier, such as a cookie ID, an IP address, a device
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identifier, or any other form of persistent unique identifier.
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(B) “Personal information” does not include publicly available
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information or deidentified data.
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(19) “Precise location information” means information derived from
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technology, including global positioning system level latitude and longitude
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coordinates and other mechanisms, that directly identifies the specific location
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of an individual with precision and accuracy within a radius of 1,750 feet.
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“Precise location information” does not include the content of communications
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or any data generated by or connected to advanced utility metering
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infrastructure systems or equipment for use by a utility.
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(20) “Process” or “processing” means any operation or set of operations
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performed on consumer health data.
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(21) “Processor” means a person who processes consumer health data
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on behalf of a regulated entity or a small business.
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(22)(A) “Publicly available information” means information that:
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(i) is lawfully made available through federal, state, or municipal
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government records or widely distributed media; and
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(ii) a regulated entity or a small business has a reasonable basis to
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believe a consumer has lawfully made available to the general public.
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(B) “Publicly available information” does not include any biometric
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data collected about a consumer by a business without the consumer’s consent.
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(23)(A) “Regulated entity” means any legal entity that:
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(i) conducts business in Vermont, or produces or provides
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products or services that are targeted to consumers in Vermont; and
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(ii) alone or jointly with others, determines the purpose and means
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of collecting, processing, sharing, or selling of consumer health data.
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(B) “Regulated entity” does not mean government agencies or
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contracted service providers when processing consumer health data on behalf
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of a government agency.
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(24)(A) “Reproductive or sexual health information” means personal
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information relating to seeking or obtaining past, present, or future
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reproductive or sexual health services.
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(B) “Reproductive or sexual health information” includes:
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(i) precise location information that could reasonably indicate a
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consumer’s attempt to acquire or receive reproductive or sexual health
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services;
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(ii) efforts to research or obtain reproductive or sexual health
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services; or
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(iii) any reproductive or sexual health information that is derived,
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extrapolated, or inferred, including from nonhealth information, such as proxy,
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derivative, inferred, emergent, or algorithmic data.
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(25) “Reproductive or sexual health services” means health services or
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products that support or relate to a consumer’s reproductive system or sexual
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well-being, including:
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(A) individual health conditions, status, diseases, or diagnoses;
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(B) social, psychological, behavioral, and medical interventions;
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(C) health-related surgeries or procedures, including abortions;
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(D) use or purchase of medication, including medications for the
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purposes of abortion;
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(E) bodily functions, vital signs, symptoms, or measurements of the
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information described in this subdivision (25);
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(F) diagnoses or diagnostic testing, treatment, or medication;
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(G) medical or nonmedical services related to and provided in
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conjunction with an abortion, including associated diagnostics, counseling,
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supplies, and follow-up services; and
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(H) any other services included in the definition of “reproductive
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health care services” in 1 V.S.A. § 150.
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(26)(A) “Sell” or “sale” means the exchange of consumer health data for
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monetary or other valuable consideration.
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(B) “Sell” or “sale” does not include the exchange of consumer
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health data for monetary or other valuable consideration:
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(i) to a third party as an asset that is part of a merger, acquisition,
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bankruptcy, or other transaction in which the third party assumes control of all
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or part of the regulated entity’s or the small business’s assets and complies
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with the requirements and obligations in this chapter; or
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(ii) by a regulated entity or a small business to a processor when
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such exchange is consistent with the purpose for which the consumer health
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data was collected and the exchange was disclosed to the consumer.
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(27)(A) “Share” or “sharing” means to release, disclose, disseminate,
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divulge, make available, provide access to, license, or otherwise communicate
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orally, in writing, or by electronic or other means consumer health data by a
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regulated entity or a small business to a third party or affiliate.
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(B) The term “share” or “sharing” does not include:
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(i) the disclosure of consumer health data by a regulated entity or
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a small business to a processor when the sharing is to provide goods or
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services in a manner consistent with the purpose for which the consumer health
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data was collected and the exchange was disclosed to the consumer;
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(ii) the disclosure of consumer health data to a third party with
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whom the consumer has a direct relationship when:
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(I) the disclosure is for purposes of providing a product or
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service requested by the consumer;
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(II) the regulated entity or the small business maintains control
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and ownership of the data; and
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(III) the third party uses the consumer health data only at the
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direction of the regulated entity or the small business and consistent with the
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purpose for which it was collected and consented to by the consumer; or
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(iii) the disclosure or transfer of personal data to a third party as an
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asset that is part of a merger, acquisition, bankruptcy, or other transaction in
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which the third party assumes control of all or part of the regulated entity’s or
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the small business’s assets and complies with the requirements and obligations
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in this chapter.
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(28) “Small business” means a regulated entity that satisfies one or both
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of the following thresholds:
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(A) the entity collects, processes, sells, or shares the consumer health
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data of fewer than 100,000 consumers during a calendar year; or
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(B) the entity derives less than 50 percent of its gross revenue from
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the collection, processing, selling, or sharing of consumer health data and the
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entity controls, processes, sells, or shares consumer health data of fewer than
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25,000 consumers.
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(29) “Third party” means an entity other than a consumer, regulated
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entity, processor, small business, or affiliate of the regulated entity or the small
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business.
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§ 1894. CONSUMER HEALTH DATA PRIVACY POLICY REQUIRED
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(a) Each regulated entity or each small business shall maintain a consumer
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health data privacy policy that clearly and conspicuously discloses:
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(1) the categories of consumer health data collected and the purpose for
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which the data is collected, including how the data will be used;
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(2) the categories of sources from which the consumer health data is
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collected;
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(3) the categories of consumer health data that is shared;
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(4) a list of the categories of third parties and specific affiliates with
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whom the regulated entity or small business shares the consumer health data;
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and
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(5) how a consumer can exercise the rights provided in section 1896 of
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this chapter.
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(b) A regulated entity or small business shall prominently publish a link to
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its consumer health data privacy policy on its homepage.
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(c) A regulated entity or small business shall not collect, use, or share
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additional categories of consumer health data not disclosed in the consumer
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health data privacy policy without first disclosing the additional categories and
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obtaining the consumer’s affirmative consent prior to the collection, use, or
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sharing of the consumer health data.
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(d) A regulated entity or small business shall not collect, use, or share
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consumer health data for additional purposes not disclosed in the consumer
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health data privacy policy without first disclosing the additional purposes and
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obtaining the consumer’s affirmative consent prior to the collection, use, or
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sharing of the consumer health data.
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(e) It is a violation of this subchapter for a regulated entity or small
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business to contract with a processor to process consumer health data in a
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manner that is inconsistent with the regulated entity’s or small business’s
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consumer health data privacy policy.
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§ 1895. COLLECTION AND SHARING OF CONSUMER HEALTH DATA
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(a) A regulated entity or small business shall not collect any consumer
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health data except:
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(1) with consent from the consumer for such collection for a specified
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purpose; or
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(2) to the extent necessary to provide a product or service that the
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consumer to whom the consumer health data relates has requested from the
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regulated entity or small business.
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(b) A regulated entity or small business shall not share any consumer health
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data except:
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(1) with consent from the consumer for the sharing that is separate and
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distinct from the consent obtained to collect consumer health data; or
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(2) to the extent necessary to provide a product or service that the
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consumer to whom the consumer health data relates has requested from the
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regulated entity or small business.
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(c) Consent required under this section shall be obtained prior to the
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collection or sharing, as applicable, of any consumer health data, and the
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request for consent must clearly and conspicuously disclose:
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(1) the categories of consumer health data collected or shared;
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(2) the purpose of the collection or sharing of the consumer health data,
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including the specific ways in which it will be used;
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(3) the categories of entities with whom the consumer health data is
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shared; and
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(4) how the consumer can withdraw consent from future collection or
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sharing of the consumer’s health data.
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(d) A regulated entity or small business shall not unlawfully discriminate
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against a consumer for exercising any rights included in this chapter.
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§ 1896. CONSUMER RIGHTS
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(a) A consumer has the right to confirm whether a regulated entity or a
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small business is collecting, sharing, or selling consumer health data regarding
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the consumer and to access that data, including a list of all third parties and
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affiliates with whom the regulated entity or small business has shared or sold
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the consumer’s health data and an active e-mail address or other online
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mechanism that the consumer may use to contact these third parties.
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(b) A consumer has the right to withdraw consent from a regulated entity’s
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or small business’s collection and sharing of consumer health data regarding
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the consumer.
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(c) A consumer has the right to have consumer health data regarding the
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consumer deleted and may exercise that right by informing the regulated entity
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or small business of the consumer’s request for deletion.
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(1) A regulated entity or small business that receives a consumer’s
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request to delete any consumer health data regarding the consumer shall:
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(A) delete the consumer health data from its records, including from
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all parts of the regulated entity’s or small business’s network, including
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archived or backup systems pursuant to subdivision (3) of this subsection (c);
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and
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(B) notify all affiliates, processors, contractors, and other third parties
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with whom the regulated entity or the small business has shared consumer
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health data of the deletion request.
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(2) All affiliates, processors, contractors, and other third parties that
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receive notice of a consumer’s deletion request shall honor the consumer’s
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deletion request and delete the consumer health data from its records in
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accordance with the requirements of this subchapter.
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(3) If consumer health data that a consumer requests to be deleted is
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stored on archived or backup systems, then the request for deletion may be
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delayed to enable restoration of the archived or backup systems, provided that
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the delay shall not exceed six months from the date of authentication of the
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deletion request.
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(d) A consumer may exercise the rights set forth in this chapter by
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submitting a request to a regulated entity or small business at any time. The
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request may be made by a secure and reliable means established by the
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regulated entity or small business and described in its consumer health data
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privacy policy. The method shall take into account the ways in which
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consumers normally interact with the regulated entity or small business, the
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need for secure and reliable communication of such requests, and the ability of
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the regulated entity or the small business to authenticate the identity of the
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consumer making the request. A regulated entity or small business shall not
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require a consumer to create a new account in order to exercise consumer
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rights pursuant to this subchapter but may require a consumer to use an
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existing account.
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(e) If a regulated entity or small business is unable to authenticate the
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request using commercially reasonable efforts, the regulated entity or small
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business is not required to comply with a request to initiate an action under this
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section and may request that the consumer provide additional information
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reasonably necessary to authenticate the consumer and the consumer’s request.
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(f) Information provided in response to a consumer request shall be
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provided by a regulated entity or small business free of charge, up to twice
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annually per consumer. If requests from a consumer are manifestly unfounded,
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excessive, or repetitive, the regulated entity or small business may charge the
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consumer a reasonable fee to cover the administrative costs of complying with
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the request or decline to act on the request. The regulated entity or small
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business bears the burden of demonstrating the manifestly unfounded,
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excessive, or repetitive nature of the request.
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(g) A regulated entity or small business shall comply with a consumer’s
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requests under subsections (a) through (c) of this section without undue delay,
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but in all cases within 45 days following receipt of the request submitted
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pursuant to the methods described in this section. A regulated entity or small
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business shall promptly take steps to authenticate a consumer request;
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provided, however, that completion of these steps does not extend the
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regulated entity’s or small business’s duty to comply with the consumer’s
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request within 45 days following receipt of the consumer’s request. The
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response period may be extended once by 45 additional days when reasonably
9
necessary, taking into account the complexity and number of the consumer’s
10
requests, provided the regulated entity or small business informs the consumer
11
of any such extension within the initial 45-day response period, together with
12
the reason for the extension.
13
(h) A regulated entity or small business shall establish a process for a
14
consumer to appeal the regulated entity’s or small business’s refusal to take
15
action on a request within a reasonable period of time after the consumer’s
16
receipt of the decision. The appeal process shall be conspicuously available
17
and similar to the process for submitting requests to initiate action pursuant to
18
this section. Within 45 days following receipt of an appeal, a regulated entity
19
or small business shall inform the consumer in writing of any action taken or
20
not taken in response to the appeal, including a written explanation of the
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reasons for the decisions. If the appeal is denied, the regulated entity or small
1
business shall also provide the consumer with an online mechanism, if
2
available, or other method through which the consumer may contact the Office
3
of the Attorney General to submit a complaint.
4
§ 1897. PROTECTION OF CONSUMER HEALTH DATA
5
A regulated entity or small business shall:
6
(1) restrict access to consumer health data by the regulated entity’s or
7
small business’s employees, processors, and contractors to only those
8
employees, processors, and contractors for whom access is necessary to further
9
the purposes for which the consumer provided consent or where necessary to
10
provide a product or service that the consumer to whom such consumer health
11
data relates has requested from the regulated entity or small business; and
12
(2) establish, implement, and maintain administrative, technical, and
13
physical data security practices that, at a minimum, satisfy reasonable
14
standards of care within the regulated entity’s or small business’s industry to
15
protect the confidentiality, integrity, and accessibility of consumer health data
16
appropriate to the volume and nature of the consumer health data at issue.
17
§ 1898. PROCESSORS OF CONSUMER HEALTH DATA
18
(a)(1) A processor may process consumer health data only pursuant to a
19
binding contract between the processor and the regulated entity or small
20
business that sets forth the processing instructions and limits the actions the
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processor may take with respect to the consumer health data it processes on
1
behalf of the regulated entity or small business.
2
(2) A processor may process consumer health data only in a manner that
3
is consistent with the binding instructions set forth in the contract with the
4
regulated entity or small business.
5
(b) To the extent possible, a processor shall use appropriate technical and
6
organizational measures to assist the regulated entity or small business in
7
fulfilling the regulated entity’s and the small business’s obligations under this
8
chapter.
9
(c) If a processor fails to adhere to the regulated entity’s or small business’s
10
instructions or processes consumer health data in a manner that is outside the
11
scope of the processor’s contract with the regulated entity or small business,
12
the processor is considered a regulated entity or small business with respect to
13
the data and is subject to all the requirements of this chapter with regard to the
14
data.
15
§ 1899. LIMITATIONS ON SALE OF CONSUMER HEALTH DATA
16
(a) It is unlawful for any person to sell or offer to sell consumer health data
17
regarding a consumer without first obtaining valid authorization from the
18
consumer. The sale of consumer health data must be consistent with the valid
19
authorization signed by the consumer. This authorization shall be separate and
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distinct from the consent obtained to collect or share consumer health data, as
1
required under section 1895 of this chapter.
2
(b) A valid authorization to sell consumer health data shall be a document
3
that is consistent with this section and is written in plain language. A valid
4
authorization to sell consumer health data shall contain all of the following:
5
(1) the specific consumer health data regarding the consumer that the
6
person intends to sell;
7
(2) the name and contact information of the person collecting and selling
8
the consumer health data;
9
(3) the name and contact information of the person purchasing the
10
consumer health data from the seller identified in subdivision (2) of this
11
subsection;
12
(4) a description of the purpose for the sale, including how the consumer
13
health data will be gathered and how it will be used by the purchaser identified
14
in subdivision (3) of this subsection when sold;
15
(5) a statement that the provision of goods or services shall not be
16
conditioned on the consumer signing the valid authorization;
17
(6) a statement that the consumer has a right to revoke the valid
18
authorization at any time and a description of how to submit a revocation of
19
the valid authorization;
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(7) a statement that the consumer health data sold pursuant to the valid
1
authorization may be subject to redisclosure by the purchaser and may no
2
longer be protected by this section;
3
(8) an expiration date for the valid authorization that expires one year
4
after the consumer signs the valid authorization; and
5
(9) the signature of the consumer and date.
6
(c) An authorization is not valid if the document has any of the following
7
defects:
8
(1) the expiration date has passed;
9
(2) the authorization does not contain all of the information required
10
under this section;
11
(3) the authorization has been revoked by the consumer;
12
(4) the authorization has been combined with other documents to create
13
a compound authorization; or
14
(5) the provision of goods or services is conditioned on the consumer
15
signing the authorization.
16
(d) A copy of the signed valid authorization shall be provided to the
17
consumer.
18
(e) A seller or purchaser of consumer health data shall retain a copy of each
19
valid authorization for the sale of consumer health data for six years from the
20
date of its signature or the date when it was last in effect, whichever is later.
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§ 1899a. GEOFENCES PROHIBITED
1
It is unlawful for any person to implement a geofence around an entity that
2
provides in-person health care services in which the geofence is used to:
3
(1) identify or track consumers seeking health care services;
4
(2) collect consumer health data from consumers; or
5
(3) send notifications, messages, or advertisements to consumers related
6
to their consumer health data or health care services.
7
§ 1899b. VIOLATIONS; ENFORCEMENT
8
(a) A violation of this subchapter shall be deemed a violation of the
9
Consumer Protection Act, 9 V.S.A. chapter 63. The Attorney General has the
10
same authority to make rules, conduct civil investigations, enter into
11
assurances of discontinuance, and bring civil actions, and private parties have
12
the same rights and remedies, as provided under 9 V.S.A. chapter 63,
13
subchapter 1.
14
(b) Nothing in this section shall be construed to preclude or supplant any
15
other statutory or common law remedies.
16
§ 1899c. EXEMPTIONS
17
(a) This subchapter does not apply to:
18
(1) information that meets the definition of:
19
(A) protected health information for purposes of the federal Health
20
Insurance Portability and Accountability Act of 1996 and related regulations;
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(B) patient-identifying information collected, used, or disclosed in
1
accordance with 42 C.F.R. Part 2, established pursuant to 42 U.S.C. § 290dd-2;
2
or
3
(C) identifiable private information for purposes of the federal policy
4
for the protection of human subjects, 45 C.F.R. Part 46; identifiable private
5
information that is otherwise information collected as part of human subjects
6
research pursuant to the Good Clinical Practice Guidelines issued by the
7
International Council for Harmonization; the protection of human subjects
8
under 21 C.F.R. Parts 50 and 56; or personal data used or shared in research
9
conducted in accordance with one or more of the requirements set forth in this
10
subsection (a);
11
(2) information and documents created specifically for, and collected
12
and maintained as part of, the patient safety surveillance and improvement
13
system established pursuant to chapter 43A of this title;
14
(3) information and documents created for purposes of the federal
15
Health Care Quality Improvement Act of 1986, and related regulations;
16
(4) patient safety work product for purposes of 42 C.F.R. Part 3,
17
established pursuant to 42 U.S.C. §§ 299b-21–299b-26;
18
(5) information that is deidentified in accordance with the requirements
19
for deidentification set forth in 45 C.F.R. Part 164;
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(6) information originating from, and intermingled so as to be
1
indistinguishable with, information described under subdivisions (1)–(5) of
2
this subsection that is maintained by:
3
(A) a covered entity or business associate as defined by the Health
4
Insurance Portability and Accountability Act of 1996 and related regulations;
5
(B) a health care facility or health care provider, as defined in section
6
9402 of this title; or
7
(C) a program or a qualified service organization as defined by 42
8
C.F.R. Part 2, established pursuant to 42 U.S.C. § 290dd-2; or
9
(7) information used only for public health activities and purposes as
10
described in 45 C.F.R. § 164.512 or that is part of a limited data set, as defined,
11
and is used, disclosed, and maintained in the manner required, by 45 C.F.R.
12
§ 164.514.
13
(b) Personal information that is governed by and collected, used, or
14
disclosed pursuant to the following regulations, parts, titles, or acts is exempt
15
from this subchapter:
16
(1) the Gramm-Leach-Bliley Act, 15 U.S.C. § 6801 et seq. and
17
implementing regulations;
18
(2) part C of Title XI of the Social Security Act, 42 U.S.C. § 1320d et
19
seq.;
20
(3) the Fair Credit Reporting Act, 15 U.S.C. § 1681 et seq.;
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(4) the Family Educational Rights and Privacy Act, 20 U.S.C. § 1232g
1
and 34 C.F.R. Part 99; and
2
(5) the Vermont Health Benefit Exchange, 33 V.S.A. chapter 18,
3
subchapter 1, and related federal laws and Vermont rules, including 45 C.F.R.
4
§ 155.260.
5
(c) The obligations imposed on regulated entities, small businesses, and
6
processors under this subchapter shall not be construed to restrict a regulated
7
entity’s, small business’s, or processor’s ability to collect, use, or disclose
8
consumer health data to prevent, detect, protect against, or respond to security
9
incidents, identity theft, fraud, harassment, malicious or deceptive activities, or
10
any activity that is illegal under Vermont or federal law; preserve the integrity
11
or security of systems; or investigate, report, or prosecute those responsible for
12
any such action that is illegal under Vermont or federal law.
13
(d) If a regulated entity, small business, or processor processes consumer
14
health data pursuant to subsection (c) of this section, that entity shall bear the
15
burden of demonstrating that the processing qualifies for the exemption and
16
complies with the requirements of this section.
17
Sec. 2. EFFECTIVE DATE
18
This act shall take effect on January 1, 2025.
19