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Key Elements of ICH-Q10 Pharmaceutical Quality System - Webinar By GlobalCompliancePanel

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Why you should attend: This webinar will help the participants understand what a Pharmaceutical Quality System is and how to transition from the compliance systems of today to the systems outlined in the various guidance's. It will require organizations to transition from a philosophy of test quality in and do not look beyond the words in the GMPs to a more proactive philosophy that is consistent with contemporary quality standards, such as ISO, and includes concepts such as building quality into the process and product. By the end of this webinar, participants will better understand what is included in a Pharmaceutical Quality System, how their organization can transition to this type of a quality system and how the changes will impact them. Areas Covered in the Session: * The transition from a quality control focus to a quality assurance focus Click here to register for this webinar Who Will Benefit: * CEOs * Senior Management * VP of Quaaity * QA Manager * QA personnel responsible for the quality system elements
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  • Added: April, 21st 2011
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  • File size: 70.14kb
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  • Tags: code of business conduct, governance documents, compliance, compliance training, compliance webinar, fda, iso, clinical trials, john e lincoln risk management, risk assessment, management process, risk identification, risk management plan, risk manager, risk management strategies, quality guidelines, pharmaceutical technology europe, risk management, fda inspections, regulatory environment, pharmaceutical manufacturing, corporate governance, good corporate governance, corporate governance principles, audit committee, governance framework
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Content Preview
 
 
Live Webinar on
 
Key Elements of ICH-Q10 Pharmaceutical Quality System
Date & Time:
 
   
Thursday, April 28, 2011
10:00 AM PDT | 01:00 PM EDT
 
Register Now
 
Duration: 90 Minutes
Instructor: John G. Lanese
Location: Online
Price : $245.00 (for one participant)

Instructor Profile:
Why you should attend:
John G. Lanese
This webinar will help the participants understand what a
President, Lanese Group,
Pharmaceutical Quality System is and how to transition from the
Inc.
compliance systems of today to the systems outlined in the various
guidance's. It will require organizations to transition from a
John G. (Jerry) Lanese, Ph.D.
philosophy of test quality in and do not look beyond the words in the
CMC is the president of The Lanese
GMPs to a more proactive philosophy that is consistent with
Group, Inc, an independent
contemporary quality standards, such as ISO, and includes concepts
consulting service provider that
specializes in Quality Systems and
such as building quality into the process and product. By the end of
Laboratory Controls. Jerry has
this webinar, participants will better understand what is included in a
taught at the college level and
Pharmaceutical Quality System, how their organization can transition
worked in various Quality Control
to this type of a quality system and how the changes will impact
and Quality Assurance roles in small
them.
and large pharmaceutical firms. For

the last 15 years he has consulted in
 
a wide range of projects from
Areas Covered in the Session:
 
consent decree remedial actions with
large pharmaceutical firms to
l
The transition from a quality control focus to a quality assurance
systems development for a small
focus
component manufacturer. He has
lectured throughout the world to
Click here to register for this webinar
clients and for major seminar
providers. He was voted the best
presenter of the year in 2001 by the
Who Will Benefit:
Institute of Validation Technology. In
2008 he received the Kenneth
l
CEOs
Chapman Industry Recognition
Award. ...more
l
Senior Management
l
VP of Quaaity
l
QA Manager
l
QA personnel responsible for the quality system elements
Suggest a Topic
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For more information, please contact the event coordinator. We look forward to seeing you at the webinar.

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GlobalCompliancePanel
About GlobalCompliancePanel
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