We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
  • SKIP TO CONTENT
  • SKIP NAVIGATION
  • Drug News
    • Trending
    • Commercial Operations
    • GMPs
    • FDA Enforcement Actions
    • Inspections and Audits
    • Postmarket Safety
    • Quality
    • Regulatory Affairs
    • Research and Development
    • Submissions and Approvals
    • FDAnews
  • Device News
    • Trending
    • Commercial Operations
    • FDA Enforcement Actions
    • Inspections and Audits
    • Postmarket Safety
    • Quality
    • Regulatory Affairs
    • Research and Development
    • Submissions and Approvals
    • FDAnews
  • Books
    • FDAnews Books Library
    • Drug Books
    • Device Books
  • Training/Events
    • Webinar Training Pass
    • Events
    • Webinar Recordings
  • Resources
    • Form 483s Database
    • FDA Approved Drugs
  • CenterWatch
  • WCG Clinical
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » FDA’s FY 2025 User Fee Schedules Notch Increases of Up to 44 Percent

FDA’s FY 2025 User Fee Schedules Notch Increases of Up to 44 Percent

July 30, 2024
Drugs Devices Regulatory Affairs Regulatory Affairs
The FDA has posted six user fee schedules for FY 2025 on the Federal Register showing increases of up to 44 percent — the highest being for biosimilars.

To View This Article:

Login

Register
Forgot your password?

Subscribe To FDAnews

Buy This Article Now

Add this article to your cart for $25.00

Upcoming Events

  • 21Oct

    MAGI@home Clinical Research Conference 2024

Featured Products

  • FDA, FTC and DOJ Enforcement of Medical Device Regulations

    FDA, FTC and DOJ Enforcement of Medical Device Regulations

  • Using Real-World Evidence in Drug and Device Submissions

    Using Real-World Evidence in Drug and Device Submissions

Featured Stories

  • Risk of 10 Obesity-Driven Cancers Reduced by GLP-1s, Study Says

  • Three Device Areas Added to CDRH’s Device-Advancing TAP Program

  • Third Alzheimer’s Drug Gets FDA Approval, Just as Diagnostic Criteria Expand

  • Draft Guidance Covers Using URRAs in Combo Product Applications

The Revised ICH E8: A Guide to New Clinical Trial Requirements

Learn More
  • Drug Products
    • Quality
    • Regulatory Affairs
    • GMPs
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Device Products
    • Quality
    • Regulatory Affairs
    • QSR
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Clinical Products
    • Trial Design
    • Data Integrity
    • GCP
    • Inspections and Audits
    • Transparency
  • Privacy Policy
  • Do Not Sell or Share My Data
Footer Logo

212 Carnegie Center, Suite 301, Princeton, NJ 08540, USA

Phone 703.538.7600 – Toll free 888.838.5578

Copyright © 2024. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing