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Academics Natoli Institute opens at LIU to combat tabletting problems. July 2014, p. 36. Re-thinking the industry-academia connection. M. Teresa Carvajal. Back Page, March 2014, p. 48. Analytical techniques Assessing an analytical method for the dissolution profile of an extended-release tablet in accordance with QbD. Maria Maeso Puertollano, Tim Cartwright, Mike Aylott, and Nicola Kaye. January 2009, p. 30. Automating push-through force testing of blister packs. Salil Jha. May 2011, p. 7. Breaking-force tests for empty and filled hard capsules and softgels. Walter Friesendorf. Can PAT "build in" quality? Yashwant Pathak. Back Page, September 2007, p. 72. Capsules and Capsule Filling Desktop Reference, July 2010, p. 17. Capsule endoscopy for evaluation of drug delivery systems in the upper gastrointestinal tract. Pernille Barbre Pedersen, Peter Vilmann, Daniel Bar-Shalom, and Anette Müllertz. October 2012, p. 20. Characterization and modeling of softgel drying pro - cesses. Q. Fang, Y. Hu, N. Yu, S. Majuru, and M. Hariharan. May 2011, p. 24. Detecting counterfeit drug products via impurity map - ping. Aurélie Bart, Ziyang Su, Karl V. Wood, Stephen R. Byrn, and M. Teresa Carvajal. October 2009, p. 24. Embracing QbD and PAT in nutraceutical production. Misty Muscarella, Charles Preuss, Y.V. Pathak, and Adnan Sabir. October 2011, p. 18. Elemental impurities. John McCarty. Eye on Excipients, March 2013, p. 39. How to ensure your dust collection system complies with combustible-dust standards. David Steil, Tony Supine, and Mike Walters. May 2013, p. 20. Improving tablet coating yield and quality via computer- based simulations. Maxim Puchkov and Hans Leuen - berger. October 2010, p. 20; Coating Desktop Reference, July 2012, p. 24. Influence of mechanical stress on the formation of cracks in two-piece capsules. David Fulper, Haibo Wang, and Dawn Downey. January 2010, p. 8. Measuring bulk density: Advantages of a shear cell. Vinnie Hebert. October 2013, p. 31. Measuring water activity as a means to reduce microbial limit testing. Anthony J. Fontana. October 2008, p. 28. Micro-extraction technique for isolation of soluble contaminants in pharmaceutical tablets. Mary Stellmack. October 2009, p. 18. Near-infrared spectroscopy: Applications in solid dosage form analysis. Deepak Kaushik, Kumud Madan, and Harish Dureja. October 2006, p. 22. New developments in dissolution testing of tablets and capsules. Margareth R. C. Marques, William Brown, Gabriel Giancaspro, Natalia Davydova, Edith Chang, Jeanne Fringer, Walter Hauck, and Anthony DeStefano. October 2012, p. 12. Online thermal effusivity monitoring: A promising technique for determining when to conclude blending of magnesium stearate. Yves Roy, Nancy Mathis, Stephen Closs, Jason Boodram, Manuel Hervas, Mani Sunda - rarajan, Theodore Larason, and Wade Meyer. March 2005, p. 38. Online x-ray inspection of filled capsules. Melanie Beck, Martin Vogt, and Iulian Maga. January 2012, p. 12. Powder blenders and NIR: A brief overview. Matthew N. Bahr. May 2008, p. 38. A rapid vehicle-screening approach for formulating a low-solubility compound into liquid-filled capsules. Amol Kheur, Anil Kane, Mohammad Aleem, Maureen McLaughlin, Kiran Kumar Tumbalam, and Shivaprakash Poojary. January 2014, p. 10. Recent challenges in dissolution testing, including USP initiatives. Vivian A. Gray, January 2012, p. 28. Reducing risk in the development and manufacture of tablets using rapid compressibility assessments. Dipankar Dey and Michael Gamlen. September 2011, p. 28. The role of NIR spectroscopy in meeting the PAT challenge. Frederick H. Long. March 2007, p. 20. A simple test to differentiate gelatin from hypromellose capsules. Enrique Requejo Gabás, Fernando Díez Menendez, Luis Polo Díez, and Nour Kayali. July 2013, p. 16. Simulated tabletting, real-world pay-off. Kendal Pitt. Back Page, September 2010, p. 56. Testing powder flowability. Robert G. McGregor. March 2011, p. 20. Tooling supplier, university seek cure for sticking. July 2013, p. 40. Update on the FDA's spectral library of excipients. Philip H. Merrell, Lucinda Buhse, and Jason D. Rodriguez. July 2013, p. 27. Using an automated workstation to improve operations and simplify investigations. C.J. Moynihan and Robert C. Houser. May 2012, p. 23. Using low-field MRI to improve tablet dissolution testing. James Butler and Kevin Nott. January 2010, p. 25. Using stable isotopes to authenticate pharmaceutical materials. John P. Jasper. May 2004, p. 37. index to articles 2003-2014 i n d e x t o a r t i c l e s Tablets & Capsules November 2013 7