FDA Regulations for instrument Qualification and Validation Processes

  • 150.00 Dollar US$
  • Published date: February 21, 2017
    • Fremont, California, United States

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

Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501119LIVE?channel=mailer&camp=Webinar&AdGroup=marketplace_Apr_2017_SEO

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