FDA Regulations for Qualification and Validation Processes - 2017

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: [email protected]

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WHEN AND WHERE

28 April 2017
United States of America

ORGANIZER

Compliance4All

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Added 7 years ago by Compliance4All on Education , Health and Medicine , Health , Public Health