Analytical Instrument Qualification and Validation Processes - 2017
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 and Presenter Information
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.
Relevant Government Agencies
Validation Processes
Event Type
Webcast
This event has no exhibitor/sponsor opportunities
When
Tue, Oct 17, 2017, 10:00am - 11:00am
PT
Cost
| Live Webinar: | $150.00 |
| Recorded Webinar: | $190.00 |
Website
Click here to visit event website
Organizer
NetZealous - Compliance4All
