Measuring Blood Pressure in Clinical Practice: We Can and Must Do Better J. Rick Turner Editorial 30 December 2018 Pages: 685 - 686
European Pharma Oligonucleotide Consortium A Move to Consolidate Oligonucleotide Knowledge and Share Experience Within the Community Anna TivestenNadim AkhtarThomas Eichinger Letter to the Editor 30 December 2018 Pages: 687 - 688
Value of IRB in Expanded Access Richard KleinMarjorie A. Speers Letter to the Editor 30 December 2018 Pages: 689 - 689
Clinical Study Design to Assess Both Short- and Long-term Efficacy in Addition to Group Sequential Test on Safety Jiacheng YuanPeter MesenbrinkGary Koch Biostatistics: Original Article 30 December 2018 Pages: 690 - 695
The Safety Explorer Suite: Interactive Safety Monitoring for Clinical Trials Jeremy WildfireRyan BaileyJack G. Modell Clinical Trials: Original Article 30 December 2018 Pages: 696 - 700
CRISPR-Cas9: A Precise Approach to Genome Engineering Jorge E. SimónÁngel S. RodríguezNelson Santiago Vispo Clinical Trials: Review 30 December 2018 Pages: 701 - 707
Advancing the Practice of CRCs Why Professional Development Matters Linda S. Behar-HorensteinAlena PrikhidkoH. Robert Kolb Educational Perspectives: Original Article 30 December 2018 Pages: 708 - 717
Anticancer Drug Prescription Patterns in Japan: Future Directions in Cancer Therapy Shoyo ShibataMaiko MatsushitaTakeshi Suzuki Global Perspectives: Original Article 30 December 2018 Pages: 718 - 723
What Drives Adoption of National Labels as Global Reference Labels? A Case Study With the JPI Shimon YoshidaRie MatsuiChikara Kikuchi Global Perspectives: Original Article 30 December 2018 Pages: 724 - 730
Relationship Between the Review Time and Various PMDA Consultations in Recent New Drug Approval Cases in Japan Keiji NishiyamaSatoshi ToyoshimaNaomi Nagai Global Perspectives: Original Article 30 December 2018 Pages: 731 - 738
Recent Advances in Drug Development and Regulatory Science in China Jie ChenNaiqing Zhao Global Perspectives: Original Article 30 December 2018 Pages: 739 - 750
Strengthening Health Products Regulatory Systems to Enhance Access to Quality Health Products in the Asia-Pacific John C. W. Lim Global Perspectives: Commentary 30 December 2018 Pages: 751 - 754
Incremental Cost-Effectiveness Ratio and Net Monetary Benefit: Promoting the Application of Value-Based Pricing to Medical Devices—A European Perspective Andrea MessoriSabrina Trippoli Global Perspectives: Letter to the Editor 30 December 2018 Pages: 755 - 756
Patient Reporting of Adverse Drug Reactions (ADRs): Survey of Public Awareness and Predictors of Confidence to Report Vidhya HarirajZoriah Aziz Product Safety: Original Article 30 December 2018 Pages: 757 - 763
Survey of Safety Information in the Investigator’s Brochure: Inconsistencies and Recommendations Michael Jacob KlepperLeander Fontaine Product Safety: Original Article 30 December 2018 Pages: 764 - 770
Outdated Prescription Drug Labeling: How FDA-Approved Prescribing Information Lags Behind Real-World Clinical Practice Michael B. SheaMark StewartEllen Sigal Regulatory Science: Original Article 30 December 2018 Pages: 771 - 777
The Use of Real-World Evidence and Data in Clinical Research and Postapproval Safety Studies Mary Jo LambertiWayne KubickKen Getz Regulatory Science: Original Article 30 December 2018 Pages: 778 - 783
Product Approvability Recommendations From FDA Advisory Committees: Inconsistently Sought, Indirectly Obtained Joseph V. GulfoJason BriggemanAsmaa Gamie Regulatory Science: Original Article 30 December 2018 Pages: 784 - 792
Regional Approaches to Expedited Drug Development and Review: Can Regulatory Harmonization Improve Outcomes? Elizabeth RichardsonGregory DanielJonathan P. Jarow Regulatory Science: Meeting Report 30 December 2018 Pages: 793 - 798