VigiBase, the WHO Global ICSR Database System: Basic Facts Marie Lindquist Adverse Events 30 December 2008 Pages: 409 - 419
Good Practices for Handling Adverse Events Detected through Patient Registries Nancy A. DreyerNeha ShethRichard E. Gliklich Adverse Events 30 December 2008 Pages: 421 - 428
Sample Size Algorithms in Clinical Trials Chien-Hua WuShu-Mei WanChiung-Yu Huang Biostatistics 30 December 2008 Pages: 429 - 439
Urn-Based Response Adaptive Procedures and Optimality Rahul Bhattacharya Biostatistics 30 December 2008 Pages: 441 - 448
Some Guidelines for Interim Data Review of Clinical Trial Data Dennis W. KingJeremy D. Jokinen Biostatistics 30 December 2008 Pages: 449 - 453
Implementation of a Phase 1 Adaptive Clinical Trial in a Treatment of Type 2 Diabetes Fabián S. TibaldiBenoit H. L. BeckAlun Bedding Biostatistics 30 December 2008 Pages: 455 - 465
On the Amendments of China’s Provisions for Drug Registration Naiqing ZhaoChen YaoJie Chen Regulatory Affairs 30 December 2008 Pages: 467 - 475
Development and Establishment of Good Review Practices for Drug Products in Korea Young-Ok KimIn-Sook ParkBo-Kyung Choi Regulatory Affairs 30 December 2008 Pages: 487 - 491
The Effects of Physicians’ Financial Incentives on the Effectiveness of Taiwan’s Outpatient Drug Copayment Policy Hsuan-Lien ChuShuen-Zen LiuJames C. Romeis Pharmacoeconomics 30 December 2008 Pages: 493 - 502
Pharmacogenetics: From Bench Science to the Bedside Ted ShihManoli VourvahisJulie Papay Pharmacogenetics 30 December 2008 Pages: 503 - 513
Report of Task Force II: Best Practices in the Use of Medical Imaging Techniques in Clinical Trials Robert FordP. David Mozley Task Force Report 30 December 2008 Pages: 515 - 523
Statistical Thinking for Non-Statisticians in Drug Regulation Mark A. DeWyngaert Book Review 30 December 2008 Pages: 525 - 526