Overview:
Having a robust process to do an impact assessment of changes is critical to the change control process. In this webinar, we will explore and discuss methods to put systems in place to ensure that all changes that require impact assessments are appropriately assessed and impact addressed. The relevant regulatory topics will be addressed as well as ways to introduce a more robust process into your workflow.
Why you should Attend:
An all too common observation during a regulatory audit or during a product nonconformance investigation is that changes were made to the product through the product documentation that were actually harmful to the product performance or that proper studies were not undertaken to ensure the product continued to meet design goals. Another consequence of an inadequate change control strategy is when making changes to one product adversely impacts another product or multiple products.
Areas Covered in the Session:
Who Will Benefit:
The following professionals in the Pharmaceutical, Medical Device, or Combination Product industries with responsibilities in the following areas:
Alan M Golden has over 35 years of experience in the medical device industry, both in basic research and in quality assurance. Alan spent 31 years at Abbott Laboratories. For the first 16 years as part of diagnostics R&D, he developed recombinant proteins used in diagnostics tests, received three US patents and published numerous papers and abstracts. Alan then transitioned to a quality assurance role where in both the Abbott Diagnostics and Abbott Molecular divisions, he was responsible for quality assurance for new product development, on-market product support and operations.
Alan’s quality assurance experience extends from design control, change control, risk management, CAPA, process and test method validation and statistics. He has been lecturing on these topics worldwide for over 20 years.
Alan retired from Abbott in 2018 and now runs Design Quality Consultants, providing training, workshops and seminars in many areas of quality assurance.
Alan received his BS degree in Microbiology from the University of Michigan and his MS degree in Molecular Biology and Immunochemistry from the University of Illinois.