Simplified Controlled Studies in New Regions for Safety Concern Arising From Using Foreign Safety Data Yeong-Liang LinChien-Hua WuK. Arnold Chan Drug Safety 31 December 2006 Pages: 365 - 369
Ethical Issues for Clinical Research Managers Adil E. ShamooDavid B. Resnik Clinical Research 31 December 2006 Pages: 371 - 383
A Practical and Efficient Approach to Database Quality Audit in Clinical Trials Larry Z. ShenJay Zhou Statistics 31 December 2006 Pages: 385 - 393
On Traditional Chinese Medicine Clinical Trials Shein-Chung ChowAnnpey PongYu-Wei Chang Statistics 31 December 2006 Pages: 395 - 406
A Cost-Benefit Approach to the Amount of Experimentation in Clinical Trials Hamid PezeshkJohn Gittins Statistics 31 December 2006 Pages: 407 - 411
Development of a Drug Information Webography and Push Notification Service Kelly M. Smith Drug Information 31 December 2006 Pages: 413 - 419
PhRMA Working Group on Adaptive Designs: Introduction to the Full White Paper Paul GalloMichael Krams Adaptive Design 31 December 2006 Pages: 421 - 423
Adaptive Designs: Terminology and Classification Vladimir Dragalin Adaptive Design 31 December 2006 Pages: 425 - 435
Implementing Adaptive Designs: Logistical and Operational Considerations Judith A. QuinlanMichael Krams Adaptive Design 31 December 2006 Pages: 437 - 444
Confidentiality and Trial Integrity Issues for Adaptive Designs Paul Gallo Adaptive Design 31 December 2006 Pages: 445 - 450
Adaptive Dose-Response Studies Brenda GaydosMichael KramsAlun Bedding Adaptive Design 31 December 2006 Pages: 451 - 461
Adaptive Seamless Phase II/III Designs—Background, Operational Aspects, and Examples Jeff MacaSumon BhattacharyaMichael Krams Adaptive Design 31 December 2006 Pages: 463 - 473
Sample Size Reestimation: A Review and Recommendations Christy Chuang-SteinKeaven AndersonSylva Collins Adaptive Design 31 December 2006 Pages: 475 - 484
