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Webinars

Event 

Title:
A Quality Management System Customer Success Story with Purdue Pharma
When:
03.25.2010
Category:
Enterprise Quality Management

Description

Webinar Date:  March 25, 2010   Time:  12:00 to 12:30 PST, 3:00 to 3:30 EST

Click here to Register

Summary:

A Quality Management System Customer Success Story with Purdue Pharma

 
Join the USDM team and our featured speakers, Gino Garofalo, Director, Quality Assurance, Purdue Pharmaceuticals and Philippe Gaudreau, CEO, SOLABS to hear a first-hand account of Purdue’s Quality Management System implementation experience.

With increasing regulatory scrutiny from FDA, EMEA and other agencies, companies are scrambling to get compliant.  Learn how to accomplish this faster, more efficiently and without compromising Regulatory Exposure.

  • Review lessons learned from conception through go-live
  • Discuss industry best practices for implementation and achieving validation and FDA system compliance
  • Understand benefits gained and how SOLABS QMS software was instrumental in simplifying, unifying and optimizing Purdue’s Quality Management System
  • Learn from challenges and road blocks faced during implementation and validation and how they were addressed

Do you have the knowledge and the right tools for ensuring regulatory compliance?  Gain critical knowledge and insight into selection and implementation of a Quality Management System by attending our complimentary webinar.

Sponsored by USDM's EQM Practice.
Visit our website to register for additional EQM Webinars.

Meet your Presenters: 

Gino Garofalo, Director Quality Assurance Purdue Pharmaceuticals Canada, oversees all activities in QC, QA and Validation for Canadian operations and serves on the international Quality Advisory Group of the company. He was instrumental in leading the efforts toward the successful automation of the QMS through an integrative software and workflow solution in 2006.

Philippe Gaudreau, CEO SOLABS, founded the company more than 10 years ago. In time, he has acquired strong competencies in document management, 21 CFR Part 11 compliance and computer system validation which he continues to explore with his numerous involvements in the Industry.

Robert Lesnefy, EQM and GRC Practice Leader USDM, has over 25 years of experience in Quality Assurance & Regulatory compliance in pharmaceuticals, bio-tech, medical device, nuclear and petro-chemical industries. Bob is currently leading a global QMS implementation across 34 countries.

Webinar Date:  March 25, 2010   Time:  12:00 to 12:30 PST


Collaborate Now!  Please enter comments or questions regarding this webinar in the space provided below.  We want to know if you like the topic, what else you would like to learn about, if you would like to contribute to the presentation, if something is not relevant or interesting.  Help us shape the most effective experience.

 

 

 

 

Comments (2)Add Comment
0
a guest
March 17, 2010
193.129.185.28
...

I am interested in this webinar, but the time is not convenient (I am based in the UK). Will this be available as a recorded webinar?

Thanks

0
a guest
March 17, 2010
184.8.42.235
...

Absolutely. All webinars presented by the USDM Team of SMEs are posted to our website within 24 hours following the presentation. You will find the list of recorded webinars on the USDM Home Page - lower right side of page.

Please let me know if I can provide further information or assistance: rmeledy@usdatamanagement.com

Best Regards,
Rebecca Meledy
US Data Management

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About USDM

USDM is a leading global consulting firm focused on life sciences.  We specialize in regulated business processes, with an emphasis on compliance and performance.

USDM provides innovative services and solutions that enable life science companies to achieve and maintain compliance across the entire enterprise.