September 2014 Preview
 
 

Pharmaceutical Technology is the only peer-reviewed publication serving the largest requested circulation of 34,774 BPA-audited subscribers (December 2013 BPA Statement). Here is the September editorial lineup to give you a heads up on the coverage in this issue and to assist you in your decision to advertise in Pharmaceutical Technology this month.

Ad Close is August 11

 
 
CPHI Show Issue

Focus: QbD in API Manufacturing
Recognition of the value of a quality by design (QbD) approach continues to increase. For small-molecule API manufacturing, to successfully adopt/implement QbD, it is necessary to define the critical quality attributes for each process step. This article considers the current best practices for defining these critical quality attributes. - Cynthia A. Challener, Contributing Editor

 
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  • Pharma Q&A
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  • US Regulatory Watch
  • European Regulatory Watch
  • Inside Standards
  • Emerging Market Report: Asia
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EDITORIAL PREVIEW
September 2014

Editorial Content Subject To Change

API Synthesis and Manufacturing: Asymmetric Synthesis
Cynthia Challener, contributing editor


Formulation/Drug Delivery: Orally Inhaled and Nasal Drug Products Exploring Newly Introduced Methods For Testing Metered Dose Inhalers With Add-On Devices
Mark Copley, Copley Scientific


PEER-REVIEWED

Investigation of Various Impurities in Febuxostat
Anand M. Lahoti* PhD, Ponnaiah Ravi, PhD, Neela Praveen Kumar, PhD, V. Innareddy, P. S. Deepthi, V. Shanmugam, M. Sudhakar Rao and Vivekananda Reddy, PhD, Neuland Laboratories Ltd, Research & Development Center, Hyderabad, AP, India.

Impact of Quality by Design Tools and Processes on Development of Robust Chromatographic Methods
Melissa Hanna-Brown, Kimber Barnett, Brent Harrington, Tim Graul, Jim Morgado, Steve Colgan, Loren Wrisley, Roman Szucs, Greg Sluggett, Gregory Steeno, Jack Pellett (Pfizer, UK and Pfizer, CT USA)

BEST PRACTICES
Troubleshooting: Solid Dosage

Technical Q&A: Modular Manufacturing

Sterile Manufacturing


 

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