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:
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
Email:
[email protected]