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 Drug Weekly
    • FDAnews
  • Device News
    • Trending
    • Commercial Operations
    • FDA Enforcement Actions
    • Inspections and Audits
    • Postmarket Safety
    • Quality
    • Regulatory Affairs
    • Research and Development
    • Submissions and Approvals
    • FDAnews Device Weekly
    • 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
  • About Us
    • The Company
    • FDAnews Editorial Board
    • Contact Us
  • Advertising
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Store » Books

Search the Store

Shop By Category

Drug Products

Drug Books

Device Products

Device Books

Clinical Products

Shop By Media

Books

Webinar Recordings

Like these Titles?!

FDAnews offers an Online Books Library Subscription for year-round unrestricted access to all books and reports. They can be accessed, searched, downloaded and read on laptops and other mobile devices anywhere, anytime!

Featured Product In Books

Calculating-Sample-Size-to-Satisfy-FDA-Expectations-500.png

Calculating Sample Size to Satisfy FDA Expectations

$199.00
Regulatory authorities require risk-based sample sizes that have a sound statistical foundation. Ensure your organization can meet their expectations with Calculating Sample Size to Satisfy FDA Expectations. Read More

Books

Device Software Safety Risks: Standards Lead to Closer FDA Scrutiny

$397.00
Learn More

Use QSIT to Your Advantage in FDA Device Inspections

$397.00
Learn More

Drugmakers’ Guide to Global Quality API Manufacturing

$397.00
Learn More

6 Steps to Managing Drug and Device Customer Complaints

$99.00
Learn More

Quality Risk Management for Pharmaceuticals

$179.00
Learn More

Understanding EU Drug Safety Reporting

$397.00
Learn More

Expediting the FDA Generic Drug Approval Process

$397.00
Learn More

Achieve 510(k) Notification Success for Device Software

$397.00
Learn More

Smart Labeling Self-Audits: Prescriptions for Global Regulatory Compliance

$397.00
Learn More

Cut Drug Approval Time with a 505(b)(2)

$397.00
Learn More
Creating-Masterplan-for Dug-Warehouse-Transportation

Creating a Master Plan for Drug Warehousing, Transportation and Distribution

$99.00
Learn More

Manufacturing Sterile Products to Meet EU and FDA Guidelines

$397.00
Learn More
Previous 1 2 … 6 7 8 9 10 11 12 13 14 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 or Share My Data
Footer Logo

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

Phone 703.538.7600 – Toll free 888.838.5578

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing