Issue link: https://www.e-digitaleditions.com/i/895564
Compactability testing of excipients, part 2. Metin Çelik. Eye on Excipients, May 2009, p. 33. 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. A dose of safety: Keeping contaminants out of your prod- ucts. Ray Spurgeon, Jr. March 2008, p. 30; Tabletting Desktop Reference, March 2009, p. 50. Effect of sampling methods on vitamin D blending uni- formity. Wenming Zeng, Dan Wang, and Doug Roper. October 2016, p. 17. Elemental impurities. John McCarty. Eye on Excipients, March 2013, p. 39. Excipients in the news. Matthew Knopp. Back Page, July 2013, p. 48. How to ensure your dust collection system complies with combustible-dust standards. David Steil, Tony Supine, and Mike Walters. May 2013, p. 20. How leak-proof are your capsules? Chris Freeman and Claire Freeman. April 2017, p. 38. The human factor: Finding the behavioral pre-conditions for error. Ben Locwin. July 2014, p. 24. Identifying the right magnetic separator for removing fer- rous contaminants. Bill Dudenhoefer. April 2013, p. 28. Ingredient identity testing: The road to GMP compli- ance. Mara Whitten. April 2011, p. 32C. Leak-testing blister packages: The limitations of the blue dye method. Oliver Stauffer. October 2016, p. 33. Maintain tablet quality by inspecting these critical points. Stephen Natoli. April 2014, p. 33. Making better tablets: A QbD approach. Michael Gamlen and Joe Domingue. September 2014, p. 10. 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. Metal detectors help ensure product purity at Global Health Industries. March 2014, p. 30. A new approach to equilibrium relative humidity testing for moisture sorption studies in pharmaceutical product stability. Peter D. Moir. May 2007, p. 18. 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. Non-destructive leak detection: Stop sending profits down the drain. Brad Feldman, May 2016, p. 17. Non-destructive options for leak-testing blister packages. Philip Stevenson. October 2014, p. 30. Non-destructive test eliminates scrapped product. Blister Packaging Desktop Reference, May 2007, p. 42. Nutra applies GNC's "quality first" principle to manufac- turing. July 2013, p. 32J. ODT delivery platforms: A comparison of dissolution times. H.-Leonhard Ohrem, Guenter Moddelmog, and Roberto Ognibene. October 2010, p. 14. Online x-ray inspection of filled capsules. Melanie Beck, Martin Vogt, and Iulian Maga. January 2012, p. 12. Outsourcing Q&A: Before you take the plunge: Tips on dissolution testing. March 2008, p. 12. An overview of capsule checkweighers. Donald K. Lightfoot. January 2011, p. 8. Powder blenders and NIR: A brief overview. Matthew N. Bahr. May 2008, p. 38. Recent challenges in dissolution testing, including USP initiatives. Vivian A. Gray, January 2012, p. 28. Reduce visual inspection of capsules by building quality in. Jim Moorhead. March 2010, p. 32C. Rethinking stability testing for tablets and capsules in containers. C. Jeanne Taborsky, Kathleen Deiss, and Edward McKinley. April 2008, p. 32. The role of NIR spectroscopy in meeting the PAT chal- lenge. Frederick H. Long. March 2007, p. 20. Selecting a vibratory sieve to check-screen highly potent powders. Rob O'Connell. October 2013, p. 23. A simple test to differentiate gelatin from hypromellose cap- sules. Enrique Requejo Gabás, Fernando Díez Menendez, Luis Polo Díez, and Nour Kayali. July 2013, p. 16. Simple tests to help you develop clean-label tablets and capsules. Tim Bellio. Back Page, September 2016, p. 48. 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. Stability testing. Philip H. Merrell. Eye on Excipients, October 2012, p. 33. Testing powder flowability. Robert G. McGregor. March 2011, p. 20. Third-party auditing. Philip H. Merrell. Eye on Excipients, March 2010, p. 37. USP offers toolkit for dissolution laboratories. Will Brown. January 2008, p. 47. 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 test- ing. James Butler and Kevin Nott. January 2010, p. 25. 26 November 2017 Tablets & Capsules