Wednesday, November 8, 2023 - 10:00am to 12:00pm EST

Featuring
> Ann Gulau – Manager II, Operational Quality, Pharma Solutions, IFF
> Jennifer Putnam – Analytical R&D Senior Supervisor, Perrigo
> Priscilla Zawislak - Global Regulatory Affairs Advocacy Manager, IFF

Description
The presentation focused on:
> Fundamental principles for managing changes related to excipient manufacturing and supply
> The role of risk assessment in evaluating change
> Excipient manufacturer (maker) best practices and case studies for evaluating changes for level of significance
> Finished drug manufacturer (user) best practices and case studies for managing significant changes

Learning/Awareness Objectives
Attendees will be able to:
> Apply the principles outlined in the IPEC Significant Change Guide for Pharmaceutical Excipients
> Understand why evaluation and notification of significant change is important
> Identify the difference between a significant and non-significant change
> Implement best practices for notification of significant changes

Who should attend?
> Excipient manufacturers, users, distributors
> Regulatory affairs
> Compendial affairs
> Quality affairs

Note: Did you know this webinar may count toward continuing education credits? Check with your credentialing organization to confirm. A certificate of participation will be available for download upon completion of the webinar.