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 & Device Products
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Publications
    • Webinar Training Pass
    • eCFR and Guidances
    • Books
  • Clinical Products
  • Advertising
  • White Papers
  • Contact Us
  • About Us
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Store » Books » Internal Auditing Basics: A Guide for Drug and Device Manufacturers

Other Options

PDF Edition

$177.00

PDF Edition - 3-4 Copies (10% Off)

$159.00

PDF Edition - 5-6 Copies (15% Off)

$150.00

PDF Edition - 7-9 Copies (20% Off)

$142.00

PDF Edition - 10+ Copies (25% Off)

$133.00

Internal Auditing Basics: A Guide for Drug and Device Manufacturers

$177.00
Books

Product Details

Internal Auditing Basics
A Guide for Drug and Device Manufacturers

Internal audits are a critical element of your quality management system. Your approach must be both systematic and documented to remain compliant.

Information from an internal audit provides management with the knowledge they need to show how effectively the company maintains the quality of the product and their processes.

This FDAnews Brief is an introduction for quality management newcomers — a refresher course for more experienced staff — and a training tool for those taking on responsibility for audits.  Readers will learn about:

  • Regulators’ requirements for management review
  • Comparison of FDA regulations to ISO 9001, ASQ Quality System and ICH E10
  • Characteristics of an effective audit team
  • Scheduling and tracking audits
  • Reporting and responding to an audit

The value of an internal audit goes beyond simply regulatory compliance. It can be used to:

  • Identify problems and fix them before a regulatory inspection
  • Improve your processes
  • Train your employees
  • Identify gaps in your processes
  • Keep executive management informed

Internal Auditing Basics: A Guide for Drug and Device Manufacturers demonstrates how to build an auditing operation, including scheduling and reporting, explains regulatory requirements and discusses how to turn audit results into positive improvements.

Order Your Copy Today

PDF Edition

 

Available Format

PDF Edition — $177

Who Will Benefit

  • People new or with little experience in quality management
  • Quality Assurance
  • Quality Control
  • Regulatory Affairs
  • Auditing and compliance officers
  • Production managers
  • Training managers

Multi-user Access

Save money with a license agreement allowing significant numbers of users access to an electronic version of this book. For multi-user access to multiple titles, FDAnews offers the FDAnews Online Library — a personalized collection of FDAnews publications that is fully searchable. Contact Customer Service for a quote or more information.

Our Guarantee

Not satisfied with your publication? For the PDF version, you must notify FDAnews within 24 hours of receipt of purchase and we will refund 100 percent of your purchase price.

  • 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