Issue link: https://www.e-digitaleditions.com/i/602181
Articles in bold were published in 2015. Academics Natoli Institute opens at LIU to combat tabletting prob- lems. July 2014, p. 36. Re-thinking the industry-academia connection. M. Teresa Carvajal. Back Page, March 2014, p. 48. Adherence The advantages of alternative solid dosage forms. Thomas Hein. September 2015, p. 32. Packaging's contribution to patient adherence and cost containment. Edward J. Bauer. May 2014, p. 8. Analytical techniques Applications of NIR spectroscopy in assessing raw materials and solid dosage forms. Thomas B. Gold. March 2015, p. 10. 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. Capsules and Capsule Filling Desktop Reference, July 2010, p. 17. Can PAT "build in" quality? Yashwant Pathak. Back Page, September 2007, p. 72. Capsule endoscopy for evaluation of drug delivery sys- tems 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. Density mapping of roller-compacted ribbons using ter- ahertz spectroscopy. Mark Sullivan, David Heaps, Richard McKay, Eiji Kato, Xiao Hua Zhou, Chuan-Yu Wu, Chun-lei Pei, Jian-yi Zhang, and Serena Schiano. January 2015, p. 26. 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. Gelatin capsules and dissolution. Margareth R. C. Marques. Back Page, January 2015, p. 64. 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 Leuenberger. 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 conta- minants 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. New USP elemental impurity testing: Selecting a method. Andrew Fussell. Back Page, March 2015, p. 48. Online thermal effusivity monitoring: A promising tech- nique for determining when to conclude blending of magnesium stearate. Yves Roy, Nancy Mathis, Stephen Closs, Jason Boodram, Manuel Hervas, Mani Sundararajan, 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 chal- lenge. Frederick H. Long. March 2007, p. 20. index to articles 2005-2015 i n d e x t o a r t i c l e s Tablets & Capsules November 2015 7