Tablets & Capsules

2019 Annual Buyers Guide

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Page 13 of 147

8 November 2018 Tablets & Capsules Elemental analysis by WD-XRF: A simplified approach. Glenn Williams, Thanh Nguyen, and Nicole McNulty. March 2017, p. 27. 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 comput- er-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 contam- inants in pharmaceutical tablets. Mary Stellmack. October 2009, p. 18. New developments in dissolution testing of tablets and cap- sules. 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 x-ray inspection of filled capsules. Melanie Beck, Martin Vogt, and Iulian Maga. January 2012, p. 12. Options for conducting elemental impurities testing. Timo- thy Klock. Back Page, July 2016, p. 48. 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 McLaugh- lin, Kiran Kumar Tumbalam, and Shivaprakash Poojary. January 2014, p. 10. Recent challenges in dissolution testing, including USP ini- tiatives. 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. Articles in bold were published in 2018. All T&C arti- cles, including those not listed here, are available for download at Adherence The advantages of alternative solid dosage forms. Thomas Hein. September 2015, p. 32. Packaging's contribution to patient adherence and cost con- tainment. Edward J. Bauer. May 2014, p. 8. Pharmaceutical packaging and adherence. Ben Locwin. Back Page, May 2016, p. 48. 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. Benefits of a laser-based system to measure the solid fraction of compacted ribbons and tablets. Terry Chriss. March 2017, p. 41. Breaking-force tests for empty and filled hard capsules and softgels. Walter Friesendorf. 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 processes. Q. Fang, Y. Hu, N. Yu, S. Majuru, and M. Hariharan. May 2011, p. 24. Computed tomography: Applications for evaluating tablets and capsules. Brett Muehlhauser and Nate DeRoo. January 2016, p. 15. Density mapping of roller-compacted ribbons using tera- hertz 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 mapping. Aurélie Bart, Ziyang Su, Karl V. Wood, Stephen R. Byrn, and M. Teresa Carvajal. October 2009, p. 24. Dissolution of oil-filled softgels: Formulation and analytical development. Claudia Silva, Jose Acosta, and Diego Mon- terroza. May 2017, p. 34. Effect of sampling methods on vitamin D blending unifor- mity. Wenming Zeng, Dan Wang, and Doug Roper. Octo- ber 2016, p. 17. index to articles 2008-2018

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