Course Description
Based on USP General Chapter <1220>, this course provides an understanding of how to apply the Analytical Procedure Life Cycle approach. Participants will examine analytical procedure attributes and parameters, risks associated with procedure design, and strategies used to qualify procedures and to perform continuous performance verification. Course activities include self-paced e-learning modules, recordings of live virtual sessions, case studies to reinforce knowledge, and supplemental videos featuring various software programs.
Upon completion of this course, you will be able to:
- Define the Analytical Procedure Life Cycle, as per USP <1220>.
- Explain the importance of the Analytical Target Profile and its impact on a procedure.
- Understand the application and importance of AQbD within the APLC framework.
- Learn key aspects of the quality risk management process as applied to all stages of the APLC.
- Describe identification of critical proecdure quality attributes, critical procedure parameters, and risk assessment.
- Explain how to establish Analytical Procedure Performance Characteristics criteria.
- Learn how to define Method Operable Design Region (MODR) and establish analytical control strategies for the procedure.
- Understand how software can be used to design experiments and confirm that an analytical procedure is suitable for its intended purpose.
- Conduct procedure qualification and ongoing procedure verification.
Who should participate:
- Compendial Liaison
- QC chemist
- QA manager & staff
- QC manager
- Regulators
- R&D
Access Duration:Access to this course expires 60 days from the date of registration or until you mark the course ‘Complete’ – whichever occurs first.
The accompanying USP General Chapter(s) available as resources with this course, were official as of the date indicated in the chapter PDF. Please check www.uspnf.com for relevant updates.
USP Approved Instructor
Horacio Pappa, Ph.D.
Director, General Chapters
University of Buenos Aires
Amanda Guira