£450 per person for full day or £250 per person for half day (includes lunch and refreshments)
NanoRam Training Agenda (9:30 am – 12:30 pm)
Raman spectroscopy theory
- Raman effect fundamentals, spectral fingerprints & vibrational interpretation essentials, signal quality factors
Regulatory & compliance
- GMP/PIC/S requirements for handheld Raman, expectations for raw material identification, understanding p-value / HQI-based decision criteria, compliance documentation & audit trails
NanoRam instrument overview
- Hardware components & optical design, calibration, verification & performance checks, system capabilities and limitations
Sampling & adaptor selection
- Attachments, spectral interpretation basics, managing fluorescence and poor-quality spectra, real-world sampling tips
Software & method development
- Library creation & management, identification vs investigation modes, method optimisation: thresholds, presets, specificity, data management
Hands-on practical session
- Running standard ID tests, investigation mode for unknowns, reviewing HQI/p-value results, troubleshooting user-level issues
Mira P Training Agenda (1:00 pm – 4:30 pm)
Raman spectroscopy fundamentals
- Raman scattering principles, spectra as molecular fingerprints, key factors affecting signal quality (fluorescence, SNR, optics)
Instrument overview
- Hardware components (laser, sampling optics, spectrograph, detector), attachments & adaptors, calibration & verification overview (ASTM E1840, polystyrene)
Sampling techniques & best practices
- Avoiding fluorescence issues, ensuring consistent sampling, Interpreting live spectra and quality metrics, choosing the correct adaptor for solids, liquids, packaging
MiraCal P software training
- Connecting Mira P to MiraCal, managing users & permissions, building & editing, using Model Expert to validate training spectra, data management
Hands-on practical workshop
- Running Identification mode, running investigation mode, reviewing match results (p-value, spectral overlay), understanding spectral variance, troubleshooting common issues (fluorescence, noisy spectra, poor contact)
Performance verification & compliance
- Method development considerations, avoiding false positives/false negatives, documenting verification steps, regulatory expectations (GMP, PIC/S)