- Using near-infrared spectroscopy and chemometric modeling to simultaneously determine ibuprofen and caffeine concentration in softgels
- Water activity and moisture: The complexity and interrelationships explained
- How understanding material deformation characteristics can improve tableting process scale-up
- Identifying and mitigating unwanted particle breakage
- Using fundamental powder properties to optimize flowability
- Benefits of a laser-based system to measure the solid fraction of compacted ribbons and tablets
- Elemental analysis by WD-XRF: A simplified approach
- Leak-testing blister packages: The limitations of the blue dye method
- Tabletability, compactibility, and compressibility: What’s the difference?
- Back Page: Options for conducting elemental impurities testing
- Tablet exam: Using dynamic compaction analysis to ensure successful formulations
- Stability modeling and package selection
- Back Page: Excipient variability: A very big deal sometimes
- Back Page: New USP elemental impurity testing: Selecting a method
- Back Page: You can’t correct for randomness
- Back Page: Ideas for de-risking candidate selection
- Back Page: Parallel or sequential development?
- Back Page: Simulated tabletting, real-world pay-off
- Computed tomography: Applications for evaluating tablets and capsules
- Applications of NIR spectroscopy in assessing raw materials and solid dosage forms
- Micro-extraction technique for isolation of soluble contaminants in pharmaceutical tablets
- Update on the FDA’s spectral library of excipients
- Online thermal effusivity monitoring: A promising technique for determining when to conclude blending of magnesium stearate
- Improving tablet coating yield and quality via computer-based simulations
- Using static image analysis to size crystalline particles
- Powder blenders and NIR: A brief overview
- Eye on Excipients: What’s an impurity?
- Using terahertz spectroscopy to map tablet cores and coatings
- Near-infrared spectroscopy: Applications in solid dosage form analysis
- Using an automated workstation to improve operations and simplify investigations
- Reducing risk in the development and manufacture of tablets using rapid compressibility assessments
- A simple test to differentiate gelatin from hypromellose capsules
- Assessing an analytical method for the dissolution profile of an extended-release tablet in accordance with QbD
- Detecting counterfeit drug products via impurity mapping
- Eye on Excipients: Elemental impurities (March 2013)
- The role of NIR spectroscopy in meeting the PAT challenge
- Introduction to servo-hydraulic compaction simulators
- Using stable isotopes to authenticate pharmaceutical materials
- Measuring water activity as a means to reduce microbial limit testing
- Capsule endoscopy for evaluation of drug delivery systems in the upper gastrointestinal tract
- Measuring bulk density: Advantages of a shear cell
- The advantages of an instrumented tablet press
- Spotlight on Nutraceuticals: What standard? Investigation raises questions about DNA testing