Quality Management 2011 - Designing, Developing, & Managing the Quality Manual
Date2011-11-04
Deadline2011-11-04
VenuePalo Alto, USA - United States 
KeywordsQuality Manual;FDA Quality Manual;Quality Manual Requirements;Quality Manual Indexes;Predicate
Topics/Call fo Papers
This 5-hr training on Quality Manuals in pharmaceutical and medical device industries will outline and discuss all the elements that are required in a quality manual. It will provide new perspectives, identify potential vulnerabilities and valuable insights for developing and improving your quality manual.
Why Should You Attend:
Although the term, Quality Manual, is mentioned quite frequently in the pharmaceutical and medical device industries, are you aware that the quality manual has not always been included as a requirement in these regulations? Only in recent years has its valuable role been recognized as a tool that holds the quality system together.
Quality Manuals are very unique and specific to the organization. They reflect the organization's personality as well as their attitude toward quality. These concepts will be discussed and explained in this course.
This webinar will outline and discuss all the elements that are required in a quality manual. It will provide new perspectives and help you identify potential vulnerabilities in your existing quality manual. Attendees can gain insight for developing and improving their quality manual.
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Last modified: 2011-09-30 19:44:42
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