6-Hour Virtual Seminar on Applied Statistics for FDA Process Validation

If you are unable to see the message below, [click here to view](. [Logo]( 6-Hour Virtual Seminar [6-Hour Virtual Seminar on Applied Statistics for FDA Process Validation]( [REGISTER NOW]( This course focuses on how to establish a systematic approach to implementing statistical methodologies into a process development and validation program consistent with the FDA guidance. Date: Monday, February 24, 2020 Time: 08:00 AM PST | 11:00 AM EST Duration: 6 Hours Instructor: Richard (Rick) K. Burdick Overview: In Guidance for Industry Process Validation: General Principle and Practices, process validation is defined as, "" the collection and evaluation of data, from the process design stage through commercial production.." The guidance further delineates the 'process design stage through commercial production' into three distinct stages of the product lifecycle: [Read more..](. Who Will Benefit: This seminar is designed for pharmaceutical and biopharmaceutical professionals who are involved with product and/or process design, validation, or manufacturing/control. - Process Scientist/Engineer - Design Engineer - Product Development Engineer - Regulatory/Compliance Professional - Design Controls Engineer - Six Sigma Green Belt - Six Sigma Black Belt - Continuous Improvement Manager About Speaker: Richard (Rick) K. Burdick Emeritus Professor of Statistics, Elion Labs Richard (Rick) K. Burdick , is an Emeritus Professor of Statistics, Arizona State University (ASU), where he instructed undergraduate and graduate students for 29 years. Following his tenure at ASU, Dr. Burdick was a Quality Engineering Director for Amgen Inc. for 10 years. [Read More]( GlobalCompliancePanel 39658 Mission Boulevard, Fremont, CA 94539, USA. Toll Free: +1-800-447-9407 Fax: 302 288 6884 [www.globalcompliancepanel.com]( | [Unsubscribe]( Copyright © 2020 GlobalCompliancePanel. All rights reserved.