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.
  • SKIP TO CONTENT
  • SKIP NAVIGATION
  • Drug Products
    • Books
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Subscription Newsletters
    • Free Newsletters
    • Webinar Training Pass
    • eCFR and Guidances
  • Device Products
    • Books
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Subscription Newsletters
    • Free Newsletters
    • Webinar Training Pass
    • eCFR and Guidances
  • Clinical Products
  • Advertising
  • White Papers
  • Contact Us
  • About Us
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Store » Submissions and Approvals

Search the Store

Shop By Category

Drug Products

Drug Books

Device Products

Device Books

Clinical Products

Shop By Media

Books

Webinar Recordings

Training

Featured Product In Submissions and Approvals

Accelerating-Generic-Drug-Development

Accelerating Generic Drug Development: The FDA’s New Plan for Increasing Generic Competition

$397.00
Accelerating Generic Drug Development explains the FDA’s new policy and shows how to navigate the new pathway to approval. Read More

Submissions and Approvals

Medical Device Cybersecurity Risks & Best Practices - Webinar Recording/Transcript

$287.00
Learn More

Laboratory Developed Tests, In Vitro Diagnostics & Gene Therapies - Webinar Recording/ Transcript

$287.00
Learn More

The 510(k) Process - Webinar Recording/Transcript

$287.00
Learn More

Brexit and the Impact to Your Global Business Operations - Webinar Recording/Transcript

$287.00
Learn More
Device Software Development: A Guide to Risk Management Requirements

Device Software Development: A Guide to Risk Management Requirements

$397.00
Learn More

Understanding ISO 19011:2018 - Webinar Recording/Transcript

$287.00
Learn More

De Novo Strategies for Getting Your Medical Device Approved - Webinar Recording/ Transcript

$287.00
Learn More

Top Tips for Establishing Device Supplier Quality Metrics - Webinar Recording/Transcript

$287.00
Learn More

Corporate Compliance & Liability - Webinar Recording/Transcript

$287.00
Learn More

Commissioner Gottlieb’s FDA: His First Year and a Look Ahead - Webinar Recording/Transcript

$287.00
Learn More

MDR Adverse Event Codes for Devicemakers - Webinar Recording/Transcript

$287.00
Learn More

Digital Health Tools: What YOU Need to Know - Webinar Recording/Transcript

$287.00
Learn More
Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Next
  • 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 My Personal Information
Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 703.538.7600 – Fax 703.538.7676 – Toll free 888.838.5578

Copyright © 2021. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing