FDA Regulations for Analytical Instrument Qualification and Validation Processes
January 28, 2020 - FL USWCS Consulting Inc
subscribe@worldcomplianceseminars.com
Phone:3472825400
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. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system. Session Highlights Requirements and approaches for Analytical Instrument Qualification Risk based validation approach Going through the qualification phases User requirements, writing the specifications Testing and deviation handling Proper documentation Type and extend of qualification for USP Instrument Categories Periodic review and revalidation analytical instruments and equipment Wrap up - Final questions and answers