FDAnews Announces — New Brief — Internal Auditing Basics: A Guide for Drug and Device Manufacturers

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The value of internal audits goes beyond regulatory compliance. Internal Auditing Basics: A Guide for Drug and Device Manufacturers ebook explains how drug and device manufacturers can improve their Quality Management System.

Internal Auditing Basics:
A Guide for Drug and Device Manufacturers
**An FDAnews Brief**
http://www.fdanews.com/internalauditingbasics    

What are regulators’ requirements for management review?

What are the characteristics of an effective audit team?

These are just a couple of questions manufacturers need to answer before undertaking internal audits. Internal audits are a critical element of a drug or device manufacturers quality management system. 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 processes
  •     Train employees
  •     Identify gaps in 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.

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

FDAnews Book Details:
Internal Auditing Basics:
A Guide for Drug and Device Manufacturers
Price: $177
http://www.fdanews.com/internalauditingbasics    

Easy Ways to Order:
Online: http://www.fdanews.com/internalauditingbasics            
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

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Michelle Butler
FDANEWS
+1 (703) 538-7665
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