VALID Act of 2020
USA116th CongressHR-6102| House
| Updated: 3/5/2020
Diana DeGette
Democratic Representative
Colorado
Cosponsors (1)
Energy and Commerce Committee
- Introduced
- In Committee
- On Floor
- Passed Chamber
- Enacted
Verifying Accurate Leading-edge IVCT Development Act of 2020 or the VALID Act of 2020 This bill requires the Food and Drug Administration to regulate in vitro clinical tests (i.e., tests intended for the collection, preparation, analysis, or in vitro clinical examination of specimens from the human body in order to provide information about a disease, condition, or treatment for a disease or condition).
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Timeline
Introduced in House
Referred to the House Committee on Energy and Commerce.
Health
Administrative law and regulatory proceduresAdministrative remediesAdvisory bodiesCongressional oversightDepartment of Health and Human ServicesDrug safety, medical device, and laboratory regulationEmergency medical services and trauma careFederal preemptionFood and Drug Administration (FDA)Government information and archivesHealth technology, devices, suppliesLicensing and registrationsMedical tests and diagnostic methodsPerformance measurementUser charges and fees
VALID Act of 2020
USA116th CongressHR-6102| House
| Updated: 3/5/2020
Verifying Accurate Leading-edge IVCT Development Act of 2020 or the VALID Act of 2020 This bill requires the Food and Drug Administration to regulate in vitro clinical tests (i.e., tests intended for the collection, preparation, analysis, or in vitro clinical examination of specimens from the human body in order to provide information about a disease, condition, or treatment for a disease or condition).
View Full TextSuggested Questions
Get AI-generated questions to help you understand this bill better
Timeline
Introduced in House
Referred to the House Committee on Energy and Commerce.
Diana DeGette
Democratic Representative
Colorado
Cosponsors (1)
Energy and Commerce Committee
Health
Related Bills
- Introduced
- In Committee
- On Floor
- Passed Chamber
- Enacted
Administrative law and regulatory proceduresAdministrative remediesAdvisory bodiesCongressional oversightDepartment of Health and Human ServicesDrug safety, medical device, and laboratory regulationEmergency medical services and trauma careFederal preemptionFood and Drug Administration (FDA)Government information and archivesHealth technology, devices, suppliesLicensing and registrationsMedical tests and diagnostic methodsPerformance measurementUser charges and fees