Biosimilar Insulin Access Act of 2020
Bill journey · stage 1 of 5
Just introduced
What it doesSummary introduced in house (Sep 8, 2020)
Biosimilar Insulin Access Act of 2020
This bill establishes that, if the Food and Drug Administration (FDA) finds that an insulin is biosimilar to a reference product, the insulin shall be deemed interchangeable with the reference product. (A biological product is biosimilar to a reference product if the two products are highly similar and have no clinically meaningful differences; the reference product generally receives FDA approval first, but the biosimilar product is typically less expensive.)
Under current law, a biological product that is biosimilar to a reference product may be deemed interchangeable with the reference product only if it meets additional requirements. Current law provides that interchangeable products may be substituted for each other without the prescriber's involvement.
What just happenedSep 16, 2020
Sponsor introductory remarks on measure. (CR H4487)
Who’s behind it
- Introduced in HouseSep 8, 2020
- Sep 16, 2020IntroReferralB00100
Sponsor introductory remarks on measure. (CR H4487)
- Sep 8, 2020IntroReferralH11100
Referred to the House Committee on Energy and Commerce.
Energy and Commerce Committee - Sep 8, 2020IntroReferralIntro-H
Introduced in House
- Sep 8, 2020IntroReferral1000
Introduced in House