Course Description:USP General Chapter <621> Chromatography and
compendial HPLC practices are the focus for this course. Discussion on system
suitability parameters and adjustments allowed to the chromatographic system are
key components. Additionally, the basis of HPLC theory, column selection, and
practice will be addressed. An update on harmonization will also be covered
during the course.
Upon completion of this course, you will be able to:
- Explain the science behind the HPLC technique
- Discuss the relevance of the USP General Chapter <621> Chromatography and HPLC tests
- Identify system suitability parameters for HPLC tests
- Describe USP <621> permitted adjustment in a chromatographic system
- Discuss practical considerations of an HPLC system
Who Should Participate:
- Analytical lab managers
- Analytical scientists
- QC scientists
- Pharmaceutical scientists
- Method validation specialists
- CMC reviewers
- QA specialists
- Chromatography specialists
- Regulatory professionals
There will be a knowledge assessment at the end of the course. If this course is taken as part of the USP certificate program, you will be required to pass this knowledge assessment with a score of 80 percent to determine if your comprehension of the topics presented meets USP’s minimum requirements.The live version of this recording took place on July 28, 2022.
The accompanying USP General Chapter(s) available as resources with this on-demand course, were official as of this date. Please check www.uspnf.com for relevant updates.
Access Duration:Access to this course expires 60 days from the date of registration or until you mark the course ‘Complete’ – whichever occurs first.
USP Approved Instructor
Oscar A. Quattrocchi
USP General Chapters Expert Committee since 2005
M.Sc., University of Buenos Aires