Biostatistics In Clinical Trials
商品資訊
商品簡介
Featuring articles from the prestigious Encyclopedia of Biostatistics, many of which have been fully revised and updated to include recent developments, Biostatistics in Clinical Trials also includes up to 25% newly commissioned material reflecting the latest thinking in:
- Bayesian methods
- Benefit/risk assessment
- Cost-effectiveness
- Ethics
- Fraud
With exceptional contributions from leading experts in academia, government and industry, Biostatistics in Clinical Trials has been designed to complement existing texts by providing extensive, up-to-date coverage and introducing the reader to the research literature.
Offering comprehensive coverage of all aspects of clinical trials Biostatistics in Clinical Trials:
- Includes concise definitions and introductions to numerous concepts found in current literature
- Discusses the software and textbooks available
- Uses extensive cross-references helping to facilitate further research and enabling the reader to locate definitions and related concepts
Biostatistics in Clinical Trials offers both academics and practitioners from various disciplines and settings, such as universities, the pharmaceutical industry and clinical research organisations, up-to-date information as well as references to assist professionals involved in the design and conduct of clinical trials.
目次
Antibacterial Agent Trials.
Audit and Quality Control.
Bayesian Methods.
Benefit/Risk Assessment.
Binding or Masking.
Clinical Significance Versus Statistical Significance.
Clinical Trials, Overview.
Cluster Randomization.
Cochrane Collaboration.
Community Intervention Trials.
Compliance Assessment.
CONSORT.
Controlled Clinical Trials.
Cooperative Cancer Trials.
Cooperative Heart Disease Trials.
Cooperative Studies Program, US Department of Veterans Affairs.
Cost-effectiveness.
Covariate Imbalance, Adjustment for.
Crossover Designs.
Data and Safety Monitoring.
Data and Safety Monitoring Boards.
Data Management and Coordination.
Drug Approval and Regulation.
Drug Interactions.
Eligibility and Exclusion Criteria.
Equivalence Trials.
Ethics.
European Federation of Statisticians in the Pharmaceutical Industry (EFPSI).
European Organization for Research and Treatment of Cancer (EORTC).
Factorial Designs.
Fraud.
Group-randomization Designs.
Guidelines.
Historical Controls, Bias From.
History, Early Cancer and Heart Disease Trials.
History, Overview.
Intention-to-Treat Analysis.
International Studies of Infarct Survival (ISIS).
Medical Ethics and Statistics.
Medical Research Council (MRC) Streptomycin Trial.
Meta-analysis.
Missing Data.
Multicenter Trials.
Multiple Endpoints.
Multiplicity.
Noncompliance, Adjustment for.
Nonrandomized Trials.
NSABP and Advances in the Treatment of Breast Cancer.
Number Needed to Treat (NNT).
Outcome Measures.
Pharmaceutical Industry, Statistics in.
Phase I Trials.
Phase II Trials.
Physicians' Health Study.
Postmarketing Surveillance of New Drugs and Assessment of Risk.
Preclinical Treatment Evaluation.
Prevention Trials.
Protocols.
QUOROM.
Randomization.
Randomized Treatment Assignment.
Salk Vaccine.
Sample Size Determination.
Screening Trials.
Sequential Methods.
Society for Clinical Trials.
Software.
Statistical Review for Medical Journals.
Statistical Review for Medical Journals, Guidelines for Authors.
Statisticians in the Pharmaceutical Industry (PSI).
Surrogate Endpoints.
Textbooks.
Time-varying Treatment Effect.
Treatment--Covariate Interaction.
University Group Diabetes Program (UGDP).
Vaccine Studies.
您曾經瀏覽過的商品
購物須知
外文書商品之書封，為出版社提供之樣本。實際出貨商品，以出版社所提供之現有版本為主。部份書籍，因出版社供應狀況特殊，匯率將依實際狀況做調整。
無庫存之商品，在您完成訂單程序之後，將以空運的方式為你下單調貨。為了縮短等待的時間，建議您將外文書與其他商品分開下單，以獲得最快的取貨速度，平均調貨時間為1~2個月。
為了保護您的權益，「三民網路書店」提供會員七日商品鑑賞期(收到商品為起始日)。
若要辦理退貨，請在商品鑑賞期內寄回，且商品必須是全新狀態與完整包裝(商品、附件、發票、隨貨贈品等)否則恕不接受退貨。