Curriculum
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.