Advances in drug development technologies are yielding innovative new therapies, from potentially lifesaving medicines to lifestyle products. In recent years, however, the cost of developing new drugs has soared, and concerns over drug resistance and pharmacoeconomics have come to the fore. Adverse reactions experienced at the clinical trial level serve as a constant reminder of the importance of rigorous safety and toxicity testing. Furthermore the advent of pharmacogenomics and ‘individualized’ approaches to therapy will demand a fresh approach to drug evaluation and healthcare delivery.Clinical Pharmacology provides an essential role in integrating the expertise of all of the specialists and players who are active in meeting such challenges in modern biomedical practice.Expert Review of Clinical Pharmacology (ISSN 1751-2433) provides a forum for informed debate and critical analysis of all aspects of safety, tolerability, efficacy and therapeutic applications, in addition to covering toxicity issues, adverse reactions, pharmacoeconomics and societal issues.Coverage includes:? ADME studies and PK/PD modeling ? Novel clinical trial design and conduct ? Toxicity and carcinogenesis ? Adverse effects/reactions, drug–drug and drug–disease interactions ? Pharmacogenetics, genomics and the incorporation of new biomarkers in drug development and clinical practice ? Translational medicine ? Pharmacoepidemiology, risk management and pharmacovigilance ? Pharmacotherapy in specific patient groups, such as children, women, the immunocompromised ? Pharmacology and ethnicity ? Impact on quality of life and pharmacoeconomic issues ? Regulation of drug development and marketing ? Epidemiology and biostatisticsExpert Review of Clinical Pharmacology bridges the gap between the medical profession, clinical research and the pharmaceutical industry, providing clinical and pharmaceutical researchers, drug development specialists, physicians and other healthcare professionals with the key information they need to assist in the progress of pharmacological therapy.All reviews are subject to rigorous peer review in association with our independent panel of Editorial Board members, representing the key experts in their pharmacological specialties.

藥物開發技術的進步正在產生創新的新療法，從潛在的救生藥物到生活方式產品。然而，近年來，開發新藥的成本猛增，人們對耐藥性和藥物經濟學的擔憂也日益突出。在臨床試驗階段出現的不良反應不斷提醒人們嚴格的安全性和毒性測試的重要性。此外，藥物基因組學和“個性化”治療方法的出現，將需要一種新的藥物評估和醫療保健提供方法。臨床藥理學在整合所有在現代生物醫學實踐中積極應對此類挑戰的專家和參與者的專業知識方面發揮著重要作用。臨床藥理學專家評審（ISSN1751-2433）為安全性、耐受性、療效和治療應用的所有方面的知情辯論和關鍵分析提供了一個論壇，并涵蓋毒性問題、不良反應、藥理學和社會問題。覆蓋范圍包括：?ADME研究和PK/PD建模?新穎的臨床試驗設計和實施?毒性和致癌作用?不良反應/反應、藥物-藥物和藥物-疾病相互作用?藥物遺傳學、基因組學以及在藥物開發和臨床實踐中加入新的生物標志物?轉化醫學?藥物流行病學、風險管理和藥物警戒?針對特定患者群體的藥物治療，如兒童、婦女，免疫功能受損?藥理學和種族?對生活質量和藥物經濟問題的影響?藥品開發和營銷法規?流行病學和生物統計學臨床藥理學專家評審彌合了醫療專業、臨床研究和制藥行業之間的差距，為臨床和藥物研究人員、藥物開發專家、醫生和其他保健專業人員提供了他們需要的關鍵信息，以協助藥物治療的進展。所有的評論都需要與我們獨立的編輯委員會成員進行嚴格的同行評審，代表他們藥理學專業的關鍵專家。