“…17, 18 Each technique has its own strengths and limitations, including: a relatively high limit of detection for XRPD (>~1% typically), 5, 19 long analysis times for NMR, 16 interference by excipients and subsampling with Raman, 13, 20, 21 relatively small fields of view and the inability to probe sub-surface details for SEM. 1,7,10,22 Consequently, sensitive detection of crystallinity at low loadings deep within tablets and powders represents an important niche not easily addressed by existing common methodologies.…”