FDA Regulations for Analytical Instrument Qualification and Validation Processes - 2017

Overview:  

• Product Id : 501119
• Instructor : Joy McElroy
• Friday, April 28, 2017   |   10:00 AM PDT | 01:00 PM EDT   |   Duration: 60 Minutes  

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 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 Quality Control Lab.

Others Details

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