Training purpose selection is required.
Training plan selection is required.
Course Description
It is critical to comply with 21 CFR p11 and the principles of data integrity when working under GxP during drug development and manufacturing.
This presentation introduces a qNMR solution that enables data integrity and management of qNMR methods for the GxP environment.
This on-demand recording is from USP’s qNMR Workshop, held November 17–19, 2020, and features a presentation by Dr. Fabrice Moriaud.
Who should participate:
- Analytical chemists
- QC staff
- QA staff
- R&D staff
- Regulatory staff
Access Duration:
Access to this course expires 60 days from the date of registration or until you mark the course ‘Complete’ – whichever occurs first.