Editor’s Commentary: A Vision for the Journal’s Continued Growth J. Rick Turner Commentary 01 March 2011 Pages: 113 - 117
Medical Writing: Looking Back, Moving Forward MaryAnn Foote Medical Writing 01 March 2011 Pages: 121 - 123
Topic-based Authoring: A Content Management Paradigm for Accurate, Consistent Regulatory Documents Linda Fossati WoodMichelle Herrera FosterNancy R. Katz Medical Writing 01 March 2011 Pages: 125 - 129
Little Red Riding Hood and the Big Bad Wolf Revisited as Structured Content Linda Fossati Wood Medical Writing 01 March 2011 Pages: 131 - 135
Interpretation and Implementation of Good Publication Practice Holly Brenza ZoogTing Chang Medical Writing 01 March 2011 Pages: 137 - 144
Publishing in Academia: Woes of Authorship, Figures, and Peer Review Theodore R. Sadler Medical Writing 01 March 2011 Pages: 145 - 150
Enhancing the Clinical Professional’s Knowledge of Regulatory Documents Sherri Bowen Medical Writing 01 March 2011 Pages: 151 - 154
Requirements for Biosimilars and Interchangeable Biological Drugs in the United States—in Plain Language Suzanne M. Sensabaugh Regulatory Affairs 01 March 2011 Pages: 155 - 162
Some Controversial Issues in Clinical Trials Shein-Chung ChowLan-Yon YangYing Lu Regulatory Affairs 01 March 2011 Pages: 163 - 174
Assessment of Pharmaceutical Research and Development Productivity with a Novel Net Present Value-based Project Database Shintaro SengokuToshihide YodaAtsushi Seki Regulatory Affairs 01 March 2011 Pages: 175 - 185
A Quantitative Approach for Making Go/No-Go Decisions in Drug Development Christy Chuang-SteinSimon KirbyMohan Beltangady Biostatistics 01 March 2011 Pages: 187 - 202
Design and Size of Bioequivalence Studies for Inhaled Drugs Anders Källén Biostatistics 01 March 2011 Pages: 203 - 207
Review of Methods and Measures for Using Existing Drug Information Material for Patient Information Pratyush LohaniSurinder Jeet Singh Book Review 01 March 2011 Pages: 209 - 211