Analytical Instrument Qualification and Validation Processes - 2017

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:
Risk based Validation Approach
Going Through the Qualification Phases
User Requirements, Writing the Specifications
Testing and Deviation Handling
Proper Documentation

Who Will Benefit:
Quality Professionals
Regulatory Professionals
Compliance Professionals
Production Supervisors
Validation Engineers
Manufacturing Engineers
Production Engineers

Speaker Profile:
Joy McElroy Upon earning a degree in Zoology at North Carolina State

University, Joy made her debut in the pharmaceutical industry in 1992 at

Pharmacia & UpJohn performing Environmental Monitoring and Sterility

Testing. Her hard work allowed her to move into a supervisory role at Abbott

Laboratories where she oversaw their uality Control Lab.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
At a Glance
When 17 October 2017
Where Fremont, CA, United States
Organizer Netzealous LLC DBA - Compliance4All
Event Type conference
Official Website
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Added by Compliance4all
Added on 09 August 2017
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