When: |
28 Apr through 28 Apr 2017 | |
CFP Deadline: |
28 |
|
Where: |
Online Event | United States | |
Website URL: |
http://www.compliance4all.com/control/w_product/~product_id=501119LIVE?channel=mailer&camp=Webinar&AdGroup=brownwalker_Apr_2017_SEO | |
Sponsoring organization: |
Compliance4All | |
Categories: |
Medicine & Health - Pharmaceutical / Medicinal |
Keywords:
Event description:
Overview:
In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient.
Why Should You Attend:
The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for analytical equipment qualification and validation in your facility?
Areas Covered in the Session:
Requirements and approaches for Analytical Instrument Qualification
Risk based validation approach
Going through the qualification phases
User requirements, writing the specifications
Who Will Benefit:
Laboratory managers, supervisors and analysts
IT managers and staff
Consultants
Laboratory suppliers of material, equipment and services
Senior quality managers
Speaker Profile:
Joy McElroy Upon earning a degree in Zoology at North Caro...
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Posting date:
01 March 2017 | 153 views
Placement:
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