Pharmaceutical Applications of Solid-State NMR Spectroscopy
Registration Agenda Biographies
Let your voice be heard!
The Quantitative NMR Spectroscopy Expert Panel of The United States Pharmacopeia (USP) will be developing a new informational General Chapter on solid-state NMR (ssNMR) spectroscopy which will provide useful guidance on current scientific and regulatory approaches for the analysis of pharmaceuticals. USP will be hosting an Open Forum to discuss the use of ssNMR to characterize several critical quality attributes (CQAs) of pharmaceutical substances, products, excipients, and other materials that have been demonstrated in the literature yet not widely implemented for routine quality control.
USP invites interested stakeholders to participate in the Open Forum to discuss a developing USP General Chapter covering technical guidance and analysis of pharmaceutical CQAs by ssNMR Spectroscopy. This interactive Open Forum will be held virtually on Thursday, June 24, from 10:00 a.m. – 12:00 p.m. Eastern Standard Time. Advanced registration is free and required.
Suggested topics
- Analysis of polymorphism and crystallinity by solid-state NMR spectroscopy
- Excipient-API interactions by solid-state NMR spectroscopy
Who should participate?
- Quality control analysts
- Suppliers of raw input materials, including excipients, testing laboratories
- Regulators
- Physical, material, and biophysical analysis scientist
- Formulation and Preformulation scientists
- Material characterization scientists
For further information or to suggest additional stakeholder topics, contact Jacqueline D. Starkes at jws@usp.org