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Analytical Instrument Qualification and Validation Processes - Webinar


2017, October 17 @ 10:00 - 11:00

Clinical, Food, Pharmaceutical, Water » Webinar


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.

Visit www.compliance4all.com


Venue

Internet - webinar

Organizer

Compliance4All
Phone: +1-800-447-9407
Email: support@compliance4All.com
Visit organizer website



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