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HR 8190 116th Congress House Health Blood and blood diseases Competition and antitrust Drug safety, medical device, and laboratory regulation Drug therapy Health technology, devices, supplies Intellectual property Licensing and registrations Prescription drugs

Biosimilar Insulin Access Act of 2020

Introduced: September 8, 2020 Introduced by: Grothman, Glenn Republican · Wisconsin See on congress.gov
 Everywhere this bill has been 3 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Sep 16, 2020
Sponsor introductory remarks on measure. (CR H4487)
Sep 8, 2020
Referred to the House Committee on Energy and Commerce.
Sep 8, 2020
Introduced in House
 Plain-English summary Congressional Research Service

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's happening now September 16, 2020

Sponsor introductory remarks on measure. (CR H4487)

 Committees of jurisdiction 1