Genomic Data Protection Act

#863 | S Congress #119

Policy Area: Commerce
Subjects:

Last Action: Read twice and referred to the Committee on Commerce, Science, and Transportation. (3/5/2025)

Bill Text Source: Congress.gov

Summary and Impacts
Original Text

Bill Summary

The **Genomic Data Protection Act** is legislation aimed at safeguarding consumer rights regarding their genomic data held by direct-to-consumer genomic testing companies. It establishes several key provisions:

1. **Consumer Controls**: The Act mandates that genomic testing companies provide an easy mechanism for consumers to access, delete their accounts, and destroy their biological samples. This mechanism must be clearly communicated to consumers.

2. **Notification Requirements**: Companies must inform consumers about their rights regarding genomic data and any deidentified data that might be used for research. Additionally, if a company is acquired, consumers must be notified about how their rights will be affected under the new ownership.

3. **Request Processing**: Companies are required to process consumer requests to delete genomic data or biological samples within 30 days and inform consumers once the action has been completed. If a company is sold during this period, the new owners must still comply with these requests.

4. **Exceptions**: There are certain conditions under which companies can deny deletion requests, such as when information is required for legal reasons or regulatory compliance.

5. **Enforcement**: The Federal Trade Commission (FTC) is given the authority to enforce the provisions of this Act, treating violations as unfair or deceptive practices under existing laws.

6. **Definitions**: The Act provides clear definitions for terms like "genomic data," "biological sample," and "direct-to-consumer genomic testing company," ensuring clarity in its application.

7. **Legal Relationship**: The Act preserves existing federal and state laws, ensuring it does not override other legal protections unless there is a direct conflict.

Overall, the Genomic Data Protection Act enhances consumer autonomy over genomic data, ensuring privacy and security in the face of growing genomic testing services.

Possible Impacts

Here are three examples of how the **Genomic Data Protection Act** could affect people:

1. **Enhanced Control Over Personal Data**:
Consumers will have the right to delete their genomic data and request the destruction of any associated biological samples. This means individuals can take control of their genetic information, ensuring that it is not stored or misused by genomic testing companies after they no longer wish to be associated with the service. For instance, a person who undergoes genetic testing and later changes their mind about sharing that information can effectively remove it from the company’s records.

2. **Informed Decision-Making**:
The Act requires genomic testing companies to provide consumers with clear notifications about their rights regarding genomic data, including how it may be shared for research. This transparency empowers consumers to make informed choices about participating in genomic testing and whether they want their data to be utilized in research. For example, a consumer may decide not to proceed with a test if they are not comfortable with how their data might be used.

3. **Consumer Protection and Legal Recourse**:
The enforcement provisions of the Act grant the Federal Trade Commission (FTC) the authority to treat violations of consumer rights regarding genomic data as unfair or deceptive practices. This means consumers have a legal framework to pursue action against companies that fail to comply with the law, providing an avenue for accountability. For example, if a company does not fulfill a consumer's request to delete their genomic data, the consumer can report this to the FTC and seek legal recourse.

[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[S. 863 Introduced in Senate (IS)]

<DOC>






119th CONGRESS
  1st Session
                                 S. 863

 To provide consumers with the right to delete their genomic data, and 
                          for other purposes.


_______________________________________________________________________


                   IN THE SENATE OF THE UNITED STATES

                             March 5, 2025

Mr. Cassidy (for himself and Mr. Peters) introduced the following bill; 
    which was read twice and referred to the Committee on Commerce, 
                      Science, and Transportation

_______________________________________________________________________

                                 A BILL


 
 To provide consumers with the right to delete their genomic data, and 
                          for other purposes.

    Be it enacted by the Senate and House of Representatives of the 
United States of America in Congress assembled,

SECTION 1. SHORT TITLE.

    This Act may be cited as the ``Genomic Data Protection Act''.

SEC. 2. CONSUMER RIGHTS REGARDING PRIVACY OF GENOMIC DATA.

    (a) Requirements.--
            (1) Consumer controls.--
                    (A) In general.--A direct-to-consumer genomic 
                testing company shall provide a simple and effective 
                mechanism to allow a consumer to--
                            (i) access the genomic data of the 
                        consumer; and
                            (ii) subject to paragraph (4)--
                                    (I) delete the account of the 
                                consumer, including any genomic data 
                                associated with such account; and
                                    (II) request the destruction of any 
                                biological sample of the consumer.
                    (B) Required mechanism.--The direct-to-consumer 
                genomic testing company shall make available to a 
                consumer the mechanism described in subparagraph (A) 
                through the primary means by which the company 
                communicates with the consumer.
            (2) Notification.--
                    (A) Consumer controls and use of deidentified 
                genomic data.--A direct-to-consumer genomic testing 
                company shall make available, in a clear and 
                conspicuous, not misleading, and easy-to-read manner a 
                notice that--
                            (i) provides a detailed and accurate 
                        representation of the rights set forth in 
                        clauses (i) and (ii) of paragraph (1)(A); and
                            (ii) discloses that the deidentified 
                        genomic data of a consumer may be shared or 
                        disclosed to conduct medical or scientific 
                        research, consistent with the privacy 
                        regulations promulgated under section 264(c) of 
                        the Health Insurance Portability and 
                        Accountability Act of 1996 (42 U.S.C. 1320d-2 
                        note).
                    (B) Purchase of company.--In the event that a 
                direct-to-consumer genomic testing company is purchased 
                or otherwise acquired by another entity, the direct-to-
                consumer genomic testing company shall send to each 
                consumer, not fewer than 30 days prior to the date on 
                which the purchase or acquisition is complete, a notice 
                that includes--
                            (i) the identity of the entity purchasing 
                        or otherwise acquiring the company; and
                            (ii) a detailed and accurate representation 
                        of the how a consumer can exercise the rights 
                        set forth in clauses (i) and (ii) of paragraph 
                        (1)(A) under the new ownership.
            (3) Processing of deletion or destruction requests.--
                    (A) In general.--With respect to a consumer's 
                request to delete the genomic data or to destroy the 
                biological sample of the consumer, a direct-to-consumer 
                genomic testing company shall--
                            (i) fulfill such request not later than 30 
                        days after the date on which the consumer makes 
                        such request; and
                            (ii) notify the consumer of such deletion 
                        or destruction not later than 30 days after the 
                        deletion or destruction.
                    (B) Outstanding requests during purchase of 
                company.--In the event that a direct-to-consumer 
                genomic testing company is purchased or otherwise 
                acquired by another entity while a consumer's request 
                to delete the genomic data or to destroy the biological 
                sample of the consumer is outstanding--
                            (i) the entity that is purchasing or 
                        otherwise acquiring the company shall comply 
                        with the requirements described in subparagraph 
                        (A); and
                            (ii) the 30-day period to fulfill such 
                        request shall begin on the date on which the 
                        consumer makes such request to the direct-to-
                        consumer genomic testing company.
            (4) Exceptions.--A direct-to-consumer genomic testing 
        company shall not permit a consumer to exercise a right 
        described in paragraph (1)(A)(ii) if the company determines 
        that the exercise of the right would require the deletion of 
        information--
                    (A) subject to a warrant, lawfully executed 
                subpoena, or other court order; or
                    (B) the company is required to retain in order to 
                comply with any other applicable legal or regulatory 
                requirement.
    (b) Enforcement.--
            (1) Unfair or deceptive acts or practices.--A violation of 
        this section or a regulation promulgated thereunder shall be 
        treated as a violation of a rule defining an unfair or 
        deceptive act or practice under section 18(a)(1)(B) of the 
        Federal Trade Commission Act (15 U.S.C. 57a(a)(1)(B)).
            (2) Powers of the commission.--
                    (A) In general.--The Commission shall enforce this 
                section in the same manner, by the same means, and with 
                the same jurisdiction, powers, and duties as though all 
                applicable terms and provisions of the Federal Trade 
                Commission Act (15 U.S.C. 41 et seq.) were incorporated 
                into and made a part of this section.
                    (B) Privileges and immunities.--Any person who 
                violates this section or a regulation promulgated 
                thereunder shall be subject to the penalties and 
                entitled to the privileges and immunities provided in 
                the Federal Trade Commission Act (15 U.S.C. 41 et 
                seq.).
                    (C) Authority preserved.--Nothing in this section 
                shall be construed to limit the authority of the 
                Commission under any other provision of law.
                    (D) Rulemaking.--Not later than 1 year after the 
                date of enactment of this section, the Commission may 
                promulgate in accordance with section 553 of title 5, 
                United States Code, such rules as may be necessary to 
                carry out this section.
    (c) Definitions.--In this section:
            (1) Biological sample.--The term ``biological sample'' 
        means any material part of the human, discharge therefrom, or 
        derivative thereof, such as tissue, blood, urine, or saliva, 
        known to contain deoxyribonucleic acid (DNA).
            (2) Commission.--The term ``Commission'' means the Federal 
        Trade Commission.
            (3) Consumer.--The term ``consumer'' means an individual 
        who provides a biological sample to a direct-to-consumer 
        genomic testing company.
            (4) Deidentified genomic data.--The term ``deidentified 
        genomic data'' means data that cannot be used to infer 
        information about, or otherwise be linked to, a particular 
        individual, provided that the business that possesses the 
        information does all of the following:
                    (A) Takes reasonable measures to ensure that the 
                information cannot be associated with a particular 
                individual.
                    (B) Publicly commits to maintain and use the 
                information only in deidentified form and not to 
                attempt to reidentify the information, except that the 
                business may attempt to reidentify the information 
                solely for the purpose of determining whether its 
                deidentification processes satisfy the requirements of 
                this subparagraph, provided that the business does not 
                use or disclose any information reidentified in this 
                process and destroys the reidentified information upon 
                completion of that assessment.
                    (C) Contractually obligates any recipients of the 
                information to take reasonable measures to ensure that 
                the information cannot be associated with a particular 
                individual and to commit to maintaining and using the 
                information only in deidentified form and not to 
                reidentify the information.
            (5) Direct-to-consumer genomic testing company.--
                    (A) In general.--The term ``direct-to-consumer 
                genomic testing company'' means a person that does any 
                of the following:
                            (i) Manufactures or develops genomic 
                        testing products or services for sale directly 
                        to consumers.
                            (ii) Analyzes or interprets genomic data 
                        obtained from a consumer.
                            (iii) Collects, uses, maintains, or 
                        discloses genomic data collected or derived 
                        from a direct-to-consumer genomic testing 
                        product or service.
                            (iv) Purchases or acquires genomic data 
                        from a direct-to-consumer genomic testing 
                        company.
                    (B) Exclusion for health care professionals.--The 
                term ``direct-to-consumer genomic testing company'' 
                shall not include a health care professional (as 
                defined in section 225 of the Public Health Service Act 
                (42 U.S.C. 234)) that performs an action described in 
                subparagraph (A) for purposes of diagnosis or treatment 
                of a medical condition.
            (6) Genomic data.--
                    (A) In general.--The term ``genomic data''--
                            (i) means any data, regardless of its 
                        format or whether the data has been 
                        deidentified, that results from the analysis of 
                        a biological sample from a consumer and 
                        concerns genomic material; and
                            (ii) includes--
                                    (I) deoxyribonucleic acids (DNA), 
                                ribonucleic acids (RNA), genes, 
                                chromosomes, alleles, genomes, 
                                alterations or modifications to DNA or 
                                RNA, and single nucleotide 
                                polymorphisms (SNPs);
                                    (II) uninterpreted data that 
                                results from the analysis of the 
                                biological sample; or
                                    (III) any information extrapolated, 
                                derived, or inferred therefrom.
                    (B) Exclusion of deidentified genomic data.--The 
                term ``genomic data'' shall not include the 
                deidentified genomic data of a consumer to the extent 
                that such data is used to conduct medical or scientific 
                research, consistent with the privacy regulations 
                promulgated under section 264(c) of the Health 
                Insurance Portability and Accountability Act of 1996 
                (42 U.S.C. 1320d-2 note).
            (7) Genomic testing product or service.--The term ``genomic 
        testing product or service'' means any testing product or 
        service that analyzes or interprets the genomic data or 
        biological sample of a consumer.
    (d) Relationship to Federal and State Laws.--
            (1) Federal law preservation.--Nothing in this Act, or a 
        regulation promulgated under this Act, shall be construed to 
        limit any other provision of Federal law, except as 
        specifically provided in this Act.
            (2) State law preservation.--Nothing in this Act, or a 
        regulation promulgated under this Act, shall be construed to 
        preempt, displace, or supplant any State law, except to the 
        extent that a provision of State law conflicts with a provision 
        of this Act, or a regulation promulgated under this Act, and 
        then only to the extent of the conflict.
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