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webinara overview
Accounting and Finance

Creating a value added Internal Audit Program

webinar description

This webinar will cover creating of a value-added an internal auditing program for complianceto FDA and ISO 13485 internal auditing requirements. It will include how to setup and manage the auditing system, as well as how to conduct an internal audit,and document the results and any non conformities. It will discuss the value of a good internal auditing program.

Reasons to attend the webinar
  • Develop or streamline an internal auditing system that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485

  • Manage an Internal Audit system and Understand the difference between internal and external audits

  • Understand what the FDA must see to verify that you are conducting your internal audits as required

Speakers:
Compliance World
Betty Lane, President
Betty Lane has over 30 years’ experience in Medical Device quality assurance and regulatory affairs. She is the founder and President of Be Quality Associates, LLC, a consulting company helping small and medium sized medical device and diagnostic companies implement and improve their quality systems. Her work enables companies to manage their business in compliance with FDA and ISO 13485 requirements, as well quality system requirements for other area such as Europe and Canada. Betty’s training experience includes over 25 years of training on all areas ISO 13485 and FDA cGMP.
10

Dec

2015

1:00 - 2:00 AM
(GMT -4)

(Duration - 60 minutes)

ATTENDANCE FEE - $199

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