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Establishes The Review Committee on Health Screen Testing for Newborns. Committee responsibilities include studying, evaluating, and making proposals regarding the potential impact of genomic…

Establishes Review Committee on Newborn Screening for purposes of studying, evaluating and making proposals related to newborn screening, including the potential impact of genomic sequencing on tests…

Parental consent is required to store, transfer, use or database DNA from any newborn child.

Creates the Parents' Bill of Rights, including the right to consent in writing before any record of a minor childs blood or DNA is created, stored or shared, except as required by Sections 1-…

Any individual, corporation, association, partnership, insurance support organization, fraternal benefit society, insurance producer, third-party administrator, self-insurer, or any other legal…

For purposes of distinguishing between or discriminating against or restricting any right or benefit otherwise due or available to an employee or prospective employee other than in connection with…

A person who maintains genetic information may not be compelled to disclose the information except under specified circumstances.

The statutes related to research apply to genetic research studies approved by an institutional review board as defined in 21 CFR, § 50 or conducted subject to the requirements of the federal common…

Group accident and sickness policies may not treat genetic information as a pre-existing condition or base eligibility or continued eligibility of any individual on health-status-related factors,…

This bill creates the Oregon Health Insurance Exchange and prohibits the treatment of genetic information in the absence of a diagnosis as a pre-existing condition in the exchange. Measure failed.…