Issue link: http://www.e-digitaleditions.com/i/751389
Sample pack boosts Moxatag launch. May 2009, p. 26. Selecting a contract packaging partner. Scott Garverick. May 2015, p. 8. Selecting an induction sealer. Cheryl Miller. April 2006, p. 34. Slat counter gives PJ Noyes an edge. May 2006, p. 30. Solving tablet stability problems using forced degradation. Dan W. Reynolds, John E. McCune, Susan G. Long, Kenneth P. Ackerman, Samuel B. Balik, William L. Canoy, Kevin L. Facchine, Mike Franklin, Angela Glendenning, Richard J. Haan, Danna M. Mattocks, Scott L. Sides, Ashley Tang, Faith Van Horn, Mickey L. Wells, and Graham Whitesell. May 2007, p. 12. Stability modeling and package selection. Matthew Knopp. May 2016, p. 11. Sustainable packaging: A primer on biopolymers and biodegradable materials. Edward J. Bauer. May 2010, p. 14; Blister Packaging Desktop Reference, July 2011, p. 22. Taste-masking medicated chewing gum. Javier Belmar. July 2014, p. 8. Time to revise CPSC protocol testing. Laura Bix, Javier de la Fuente, and Alaster Yoxall. October 2010, p. 32. Track and trace: Options for compliance. Mark Feher. May 2013, p. 12. Using sorbents to ensure drug product integrity and miti- gate risk. Chris Gilmor and Joanne B. Miechowski. January 2016, p. 27. Wide acceptance of PVC erects barrier to alternatives. Emily Nystrom. May 2009, p. 8; Blister Packaging Desktop Reference, July 2011, p. 4. Will pharmacies drive a change in packaging? Peter Mayberry. Back Page, May 2009, p. 56. Particle analysis An assessment of techniques for determining particle size during high-shear wet granulation. Kevin Macias and M. Teresa Carvajal. January 2008, p. 32. Using static image analysis to size crystalline particles. Patrick O'Hagan, Kerry Hasapidis, Vincent Chapeau, and Christian Godino. May 2008, p. 30. Powder flow Assessing how the physical properties and enhanced pow- der flow of HMPC translate to process control during direct compression of matrix tablets. True L. Rogers, Kathryn O. Hewlett, Jörg Theuerkauf, Karen M. Balwinski, and Madhusudhan Kodam. October 2014, p. 14. Fumed silica improves powder flow. Elizabeth Sims and Michael Famiglietti. Eye on Excipients, April 2016, p. 47. Measuring bulk density: Advantages of a shear cell. Vinnie Hebert. October 2013, p. 31. Preventive medicine: Keys to avoiding powder flow prob- lems. Thomas Baxter. March 2007, p. 36. Relating flow properties to process behavior in tablet presses and capsule filling machines. Kerry Johanson. May 2014, p. 28. Separation anxiety: Addressing variations in content unifor- mity data in compression processes. Thomas Baxter and James Prescott. March 2010, p. 22. Testing powder flowability. Robert G. McGregor. March 2011, p. 20. Tracking bulk density to maximize tablet production. Vinnie Hebert. March 2016, p. 27. What exactly is powder flowability? Bryan J. Ennis. Back Page, May 2006, p. 64. When powders flow like water: Addressing two-phase flow effects in tablet press feed systems. Thomas Baxter. March 2009, p. 26. Regulation, standards, and guidance Accounting for differences in TSM and EU tooling. Rich Kirk. July 2010, p. 34. 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. Assessing risk and controlling exposure to potent com- pounds during pharmaceutical packaging. John P. Farris. May 2010, p. 8. Blister technology adapts to meet regulatory and market demands. Matthew Knopp. May 2012, p. 14. The buck stops where? Clarifying responsibility under qual- ity agreements. Justin Prochnow. October 2015, p. 32B. Can PAT "build in" quality? Yashwant Pathak. Back Page, September 2007, p. 72. Chitosan as a pharmaceutical excipient? John McCarty. Eye on Excipients, September 2013, p. 51. Clearing the regulatory hurdles to bring a supplement product to market. Justin J. Prochnow. July 2010, p. 32C. Combine the TSM and ISO tooling standards. Dale Natoli. Back Page, October 2010, p. 64. Compactability testing of excipients, part 1. Metin Çelik. Eye on Excipients, April 2009, p. 42. Compactability testing of excipients, part 2. Metin Çelik. Eye on Excipients, May 2009, p. 33. Compliance challenges facing the nutraceutical and dietary-supplement industries. Joy A. Joseph. March 2009, p. 32C. Containment of high-potency drug products: Outsourcing and other challenges. Emily Nystrom. March 2010, p. 8. Contracting with the dietary supplement cGMPs in mind. Paul M. Hyman and Bryon F. Powell. September 2009, p. 32C. Creating compliant labels for dietary supplements in Canada. Peter Wojewnik. September 2010, p. 32C. Dietary supplements: Outsourcing to meet the final GMP rule. Joy A. Joseph. Back Page, March 2006, p. 72. Everyone needs a war room. Carol Brennon. Back Page, October 2008, p. 96. 20 November 2016 Tablets & Capsules