Wayne Taylor is a leading expert on the application of Statistics to the Medical Device and other FDA regulated industries. His new book Statistical Procedure for the Medical Device Industry sets the standard for applying statistics in compliance with Section §820.250, Statistical Techniques of the Code of Federal Regulations.
He is the founder and chairman of Taylor Enterprises, Inc. where he is responsible for the development of the VarTran®, Change-Point Analyzer, Sampling Plan Analyzer and Distribution Analyzer software packages as well as providing consulting and training on Statistics including Robust Design, Tolerance Analysis, Design of Experiments, Trending and Acceptance Sampling.
He is also author of the books Optimization and Variation Reduction in Quality and Guide to Acceptance Sampling. Dr. Taylor is a leading expert in Process Validation where he wrote Annex A of the Global Harmonization Task Force guideline titled Process Validation Guidance for Process Validation Engineers.
Dr. Taylor received his Ph.D. in Statistics from Purdue University where he is a distinguished alumnus. He is a fellow of the American Society for Quality, and recognized as one of 100 Notable People in the Medical Device Industry by MD&DI Magazine
Learn how to manage Statistics including establishing a policy along with procedures relative to specific areas of applications. Highlighted are statistical techniques for:
This course is designed to help you select sampling sizes and acceptance criteria for one-time studies like process validation, design verification, component qualifications and CAPA effectiveness checks including:
Learn how to manage Statistics including establishing a policy along with procedures relative to specific areas of applications.