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Application Note
FT-IR
- Differentiation of THC and CBD cannabis using FTIR
- Microanalysis in Pharmaceutical Product Development and Trouble-Shooting
- Drug Identification with FTIR
- Quality Control and Troubleshooting Pharma
- The TICTAC ATR-FT-IR Drug Library includes ATR spectra from new drugs and new psychoactive substances (NPS) / “legal highs”
- Analysis of laced Drugs
- INVENIO® R The new intuitive FTIR R&D Spectrometer
Raman Spectroscopy
- Advantages of Raman Microscopy and Imaging in Pharmaceutical QC and R&D: an in-depth Review
- Raman Characterization of the Active Pharmaceutical Ingredients (APIs) in Nasal Sprays
- Fully automated Raman measurements of pharmaceutical polymorphs and formulations
- Depth profiling of complex samples using confocal Raman microscopy
- The handheld Raman spectrometer BRAVO shares the same meticulous validation concept as any other Bruker FT-IR/NIR or Raman spectrometer
- BRAVO – The must have handheld Raman solution for Pharmaceutical Industry
- BRAVO More than compliance to Pharmaceutical regulations
- SENTERRA II Application of Raman Microscopy in Pharma
- SENTERRA II Full Compliance to Pharmaceutical Regulations
Nuclear Magnetic Resonance (NMR)
- NMR under GxP in Drug Development and Manufacturing
- NMR in Pharma: Performance Qualification (qPQ) for Quantitative NMR Applications (qNMR)
- NMR in Pharma: Application of Data Integrity Principles
- NMR in Pharma: Instrument Qualification
- Potency determination by qNMR has been shown to be a single point replacement for routine development testing which previously involved several experiments and techniques
- NMR in Pharma: The Principles of Change Control
Electron Paramagnetic Resonance (EPR)
- Pharmaceutical Applications of EPR I. Detecting and Evaluating Degradation
- Pharmaceutical Applications of EPR II. Optimizing Stability and Shelf-Life
- Pharmaceutical Applications of EPR III. Reaction MonitoringEPR
- Pharmaceutical Applications of EPR IV. Sterilization Processes
- Pharmaceutical Applications of EPR V. Paramagnetic Impurity ProfilingTransition
Total Organic Carbon
- Total Protein Determination in Pharmaceutical Products (Vaccines) by TNb Analysis on multi N/C 2100S pharma
- TOC System Suitability Test – Redefined According to New USP Regulations
- Cleaning Validation Procedures in the Pharmaceutical Industry by TOC Analysis
- Establishing Extractables Testing from Plastic Packaging Materials and Systems for Pharmaceutical Use by TOC Analysis According to USP <661>
- TOC Performance Test as per Japanese Pharmacopoeia
