Analytical Instrument Qualification and Validation Processes - 2017

  • Check with publisher
  • Published date: August 14, 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:
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: support@compliance4All.com

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