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FDA Regulations for Qualification and Validation Processes - 2017

Event Details

FDA Regulations for Qualification and Validation Processes - 2017

Time: April 28, 2017 from 10am to 11am
Location: Online
Street: 161 Mission Falls Lane, Suite 216
City/Town: Fremont
Website or Map: http://www.compliance4all.com…
Phone: 18004479407
Event Type: webinar
Organized By: Adam Fleaming
Latest Activity: Feb 24

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Event Description

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:
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
Consultants
Laboratory suppliers of material, equipment and services
Senior quality managers

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 Quality Control Lab.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

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