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Analytical Instrument Qualification and Validation Processes - 2020
Date
Oct 19, 2021 - 10:00 AM
Link to Website
Organizer
Netzealous LLC DBA - Compliance4All
Venue
online
Location
Netzealous LLC DBA - Compliance4All,
Fremont,
CA,
US,
ZIP: 94539
Phone: 18004479407
Ticket Price: $ 150.00
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]
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]
Event Categories
Keywords: Educational, HealthCare , medical