Analytical Instrument Qualification and Validation – Understanding Use of Excel and FDA Audit Preparation
February 21 - 22, 2019 - Richmond ON CAWebinar Compliance
info@webinarcompliance.com
Phone:4169154458
In this two day workshop conference 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. Additionally, case studies will explore how your management practices of your analytical equipment qualification/ validation and process validation programs can help or hurt your legal liability and the legal issues that arise from nonconformance with regulators and Auditors.