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
Laboratory suppliers of material, equipment and services
Senior quality managers
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.
Compliance4All DBA NetZealous,