Instructor:
Paula Shadle
Product ID: 700179
Training Level: Basic to Intermediate
Many firms struggle with repeated, basic errors in GMP documentation. This webinar discusses why certain types of errors are comonplace, and how to structure training, review, and feedback, to improve performance.Training alone is not effective; people need to understand the ’why’ behind the rules, or they will appear to be arbitrary. Here are strategies you can use, based on concepts of adult learning, risk management, and quality systems.
Areas Covered in the seminar:
Who Will Benefit:
This seminar will provide value to regulated companies required to follow strict documentation standards, whether GLP, GCP, or GMP. The focus will be on GMP documentation. Employees who will benefit include:
Paula Shadle, Ph.D., is the founder of Shadle Consulting, a firm that specializes in quality systems and process development for biopharmaceuticals. Dr. Shadle has over 20 years of hands-on and executive experience in biopharmaceutical process development and quality at firms including Chiron, Scios, GSK and Bayer. She has published over 40 publications and is co-inventor on 4 process patents. Dr. Shadle holds a Ph.D. degree in biochemistry from the University of California, and two years’ postdoctoral experience at the Max-Planck-Institute. She is on the boards of the West Coast Chapter, PDA, and the East Bay Chapter, AWIS, and on the editorial board of BioPharm International.
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