FDA Regulations for instrument Qualification and Validation Processes

MessageThis Webinar is over
Date Apr 28, 2017
Time 10:00 am
Cost 150.00
Online
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 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.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

 


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