Creating a value added Internal Audit Program webinar
When

December 10, 2015 @ 1:00 am - 2:00 am America/New_York
( Show in my time zone )

Organizer

Compliance World - Rahul Chakraborty

Host

Compliance World - Betty Lane

TOPICS
Attendance Fee
$199

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.

Why attend this webinar:

1. Develop or streamline an internal auditing system that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485

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

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

More information about the 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.

Recording available
Slides/PDF available