dbtreg_fda US FDA Regulatory Pathways

Subcategories of dbtreg_fda US FDA Regulatory Pathways

• dbtreg_fda_510k510(k) Premarket Notification for medical devices
• dbtreg_fda_blaBLA (Biologics License Application) for biologics
• dbtreg_fda_bpciBiosimilar pathway (BPCI Act, 351(k) applications)
• dbtreg_fda_euaEUA (Emergency Use Authorization) pathway
• dbtreg_fda_ndaNDA (New Drug Application) for small-molecule drugs
• dbtreg_fda_pmaPMA (Premarket Approval) for high-risk devices

Frequently asked questions

What is Biotechnology Regulatory Pathway Types dbtreg_fda?

Biotechnology Regulatory Pathway Types dbtreg_fda is "US FDA Regulatory Pathways". Biotechnology Regulatory Pathway Types code dbtreg_fda covers "US FDA Regulatory Pathways" at level 1 of the Biotechnology Regulatory Pathway Types hierarchy.

What does Biotechnology Regulatory Pathway Types dbtreg_fda include?

dbtreg_fda US FDA Regulatory Pathways contains 6 direct subcategories: dbtreg_fda_510k 510(k) Premarket Notification for medical devices; dbtreg_fda_bla BLA (Biologics License Application) for biologics; dbtreg_fda_bpci Biosimilar pathway (BPCI Act, 351(k) applications); dbtreg_fda_eua EUA (Emergency Use Authorization) pathway; dbtreg_fda_nda NDA (New Drug Application) for small-molecule drugs; dbtreg_fda_pma PMA (Premarket Approval) for high-risk devices.

How does Biotechnology Regulatory Pathway Types dbtreg_fda map to other classification systems?

dbtreg_fda US FDA Regulatory Pathways has equivalents in NAICS 2022 (3254, 5417). These crosswalks let you translate this code between Biotechnology Regulatory Pathway Types and 1 other classification system.

What is the parent category of dbtreg_fda?

dbtreg_fda US FDA Regulatory Pathways sits under dbtreg_fda US FDA Regulatory Pathways in the Biotechnology Regulatory Pathway Types hierarchy.