发帖
雷达卡
├── 临床科研选题：临床研究的选题设计和实施
│ ├── 21_2_14_2_种研究类型的_12_个设计要点_病例对照与临床试验研究.mp4
│ ├── 08_2_1_如何选择研究因素_对象与效应_.mp4
│ ├── 02_1_1_篇首语_7_步炼成高质量临床研究.mp4
│ ├── 01_00_试听节选_科研选题的创新性原则_实例解析_1_.mp4
│ ├── 12_2_5_研究误差来自哪里_如何规避_.mp4
│ ├── 05_1_4_8_个实例教会你从指南基金与专科诊疗中发掘选题_bilibili.mp4
│ ├── 25_3_4_如何展示临床研究结果_图形可视化_上_.mp4
│ ├── 26_3_5_如何展示临床研究结果_图形的配色与线条_下_.mp4
│ ├── 17_2_10_如何撰写临床研究计划书_.mp4
│ ├── 18_2_11_如何确定研究类型_10_大特点区分观察性和实验性研究.mp4
│ ├── 09_2_2_如何做到随机化_5_种随机抽样方法_3_种随机分组方法_bilibili.mp4
│ ├── 14_2_7_研究是否有混杂偏倚_如何控制_.mp4
│ ├── 23_3_2_离群值和缺失值的处理.mp4
│ ├── 20_2_13_3_种研究类型的_24_个设计要点_现况研究_生态学与队列研究.mp4
│ ├── 13_2_6_偏倚的来源与控制_5_种选择偏倚与_6_种信息偏倚_bilibili.mp4
│ ├── 19_2_12_如何选择合适的研究对象与数量_5_种研究类型详解.mp4
│ ├── 11_2_4_排除主观影响_盲法与重复设计_bilibili.mp4
│ ├── 15_2_8_P_值__OR__RR_与_95__CI_如何选择与确定__bilibili.mp4
│ ├── 22_3_1_临床研究数据的管理_计算变量_排序_合并拆分_转置.mp4
│ ├── 07_1_6_6_大选题切入点_结合临床诊疗路径实例解析.mp4
│ ├── 28_3_7_真实世界研究加餐.mp4
│ ├── 06_1_5_3_步确定选题_从临床工作出发_提出问题_收集资料_反复推敲_bilibili.mp4
│ ├── 10_2_3_如何设置对照组_6_种对照形式的选择_bilibili.mp4
│ ├── 03_1_2_10_个案例带你吃透好选题的_5_大原则.mp4
│ ├── 24_3_3_临床资料的_2_种分类及_5_种基本统计方法.mp4
│ ├── 27_3_6_如何展示临床研究结果_表格呈现.mp4
│ ├── 16_2_9_3_种样本量估算方法与检验效能估计_bilibili.mp4
│ ├── 04_1_3_10_个实例教会你从临床实践与文献中发掘选题_bilibili.mp4
├── 临床试验方案设计：SPIRIT规范
│ ├── SPIRIT规范的第2部分：Introduction.docx
│ ├── SPIRIT规范的第3部分：Participants，intervention，outcomes.docx
│ ├── SPIRIT规范的第1部分：Administrative Information.docx
│ ├── SPIRIT规范的第4部分Assignment of interventions.docx
│ ├── SPIRIT规范的第6部分：Monitoring.docx
│ ├── SPIRIT规范的第5部分Data collection，management，analysis.docx
├── Protocol写作入门
│ ├── 临床试验模拟
│ │ ├── Clinical Trial Simulations.pdf
│ │ ├── Simulation for designing clinical trials _ a pharmacokinetic-pharmacodynamic modeling perspective.pdf
│ ├── 生物统计附试验设计系列文章
│ │ ├── 《生物统计附试验设计》课程教学实践探讨.pdf
│ │ ├── 《生物统计附试验设计》课程教学手段改革和实践.pdf
│ │ ├── 生物统计课程考核方式的改革策略.pdf
│ │ ├── 《生物统计附试验设计》课程教学改革效果探讨.pdf
│ │ ├── 《生物统计附试验设计》课程改革探究.pdf
│ │ ├── 《生物统计附试验设计》课程教学实践探讨 (2).pdf
│ │ ├── 《生物统计与试验设计》SPOC课程建设的探索与思考．.pdf
│ │ ├── 《生物统计附试验设计》上机实验改革与实践.pdf
│ │ ├── 生物统计专业学生实践创新能力培养模式初探.pdf
│ │ ├── 建设《生物统计附试验设计》精品课程的实践与思考.pdf
│ │ ├── 项目教学法在生物统计附试验设计课程教学中的实践与思考.pdf
│ │ ├── 生物统计附试验设计课程立体化建设的探索与实践.pdf
│ │ ├── Excel在《生物统计学》双因素有重复方差分析中的应用与探讨.pdf
│ │ ├── 生物统计附试验设计课程立体化建设的探索与实践 (2).pdf
│ │ ├── 生物统计附试验设计课程教学的实践与探索.pdf
│ │ ├── 生物统计附试验设计课程考核方式的改革与实践.pdf
│ │ ├── 《生物统计及试验设计》课程教学改革探讨.pdf
│ │ ├── 生物统计与田间试验设计课程教学改革的探索和思考.pdf
│ ├── 临床试验管理类
│ │ ├── Healthy volunteers in commercial clinical drug trials _ when human beings become guinea pigs.pdf
│ │ ├── Statistical monitoring of clinical trials a unified approach.pdf
│ │ ├── Data and Safety Monitoring Committees in Clinical Trials.pdf
│ │ ├── A Practical Guide to Cluster Randomised Trials in Health Services Research.pdf
│ │ ├── Statistical Monitoring of Clinical Trials.pdf
│ │ ├── A Practical Guide to Quality Management in Clinical Trial Research (2005, Informa Healthcare).pdf
│ │ ├── A_Practical_Guide_to_Using_Qualitative reseach in RCTs(z-lib.org).pdf
│ │ ├── Design and Analysis of Clinical Trials for Predictive Medicine.pdf
│ │ ├── Communications＋Handbook＋for＋Clinical＋Trials.pdf
│ │ ├── Clinical Trials Audit Preparation_ A Guide for Good Clinical Practice (GCP) Inspections.pdf
│ ├── 肿瘤临床试验
│ │ ├── Randomized_phase_ii_cancer_clinical.pdf
│ │ ├── Cancer.Clinical.Trials.Current.and.Controversial.Issues.in.Design.and.Analysis.2016.pdf
│ │ ├── Phase I Cancer Clinical Trials.pdf
│ │ ├── A Practical Guide to Designing Phase II Trials in Oncology .pdf
│ │ ├── Cancer Clinical trial PROACTIVE STRATEGIES .pdf
│ ├── 临床统计方法综合
│ │ ├── Selected bias and Covariate Imbalances in RCTs.pdf
│ │ ├── Epidemiology and Biostatistics_ An Introduction to Clinical Research.pdf
│ │ ├── Noninferiority_testing_in_clinical_trial.pdf
│ │ ├── Clinical_Trial_Biostatistics_and_Biopharmaceutical_Applications（2015）.pdf
│ │ ├── ADVANCES IN CLINICAL TRIAL STATISTICS .pdf
│ │ ├── Analysis_of_clinical_trials_using_SAS.pdf
│ │ ├── Key Statistical Concepts in Clinical Trials for Pharma.pdf
│ │ ├── Methods_and_applications_of_statistics in clinical trial 1.pdf
│ │ ├── Multiple Analyses in Clinical Trials_ Fundamentals for Investigators.pdf
│ │ ├── Binary Data Analysis of Randomized Clinical Trials with Noncompliance.pdf
│ │ ├── Statistical_Aspects_Of_The_Design_And_Analysis_Of_Clinical_Trials_（1999）.pdf
│ │ ├── Planning and Analyzing Clinical Trials with Composite Endpoints.pdf
│ │ ├── Strategy and Statistics in Clinical Trials_ A non-statisticians guide to thinking, designing and executing.pdf
│ │ ├── Statistics Applied to Clinical Trials (第4版).pdf
│ │ ├── Modern Clinical Trial Analysis .pdf
│ │ ├── Methods and Applications of Statistics in Clinical Trials 2.pdf
│ │ ├── Inference_on_Clinical_Trials_with_Outcomes.pdf
│ │ ├── An Introduction to Statistics in early phase trial.pdf
│ │ ├── Repeated_Measures_Design_with_Generalized linear mixed models for RCTs.pdf
│ ├── 医疗器械临床试验
│ │ ├── Design, Execution, and Management of Medical Device Clinical Trials.pdf
│ │ ├── The_Design_and_ManagThe Design and Management of Medical Device clinical Trials_ Strategies and Challengeseme(z-lib.org).pdf
│ ├── 临床试验研究设计类
│ │ ├── Group Sequential Methods with Applications to Clinical Trials
│ │ │ ├── C0316_PDF_C17.pdf
│ │ │ ├── C0316_PDF_C18.pdf
│ │ │ ├── C0316_PDF_C10.pdf
│ │ │ ├── C0316_PDF_C04.pdf
│ │ │ ├── C0316_PDF_C08.pdf
│ │ │ ├── C0316_PDF_C14.pdf
│ │ │ ├── C0316_PDF_C11.pdf
│ │ │ ├── C0316_PDF_C01.pdf
│ │ │ ├── C0316_PDF_C19.pdf
│ │ │ ├── C0316_PDF_C06.pdf
│ │ │ ├── C0316_PDF_C16.pdf
│ │ │ ├── C0316_PDF_C12.pdf
│ │ │ ├── C0316_PDF_C09.pdf
│ │ │ ├── 尾页.pdf
│ │ │ ├── C0316_PDF_C13.pdf
│ │ │ ├── C0316_PDF_C05.pdf
│ │ │ ├── C0316_PDF_C07.pdf
│ │ │ ├── 首页.pdf
│ │ │ ├── C0316_PDF_C02.pdf
│ │ │ ├── C0316_PDF_C15.pdf
│ │ │ ├── C0316_PDF_C03.pdf
│ │ ├── Cluster Randomised Trials, Second Edition.pdf
│ │ ├── Group Sequential and Confirmatory Adaptive Designs in Clinical Trials.pdf
│ │ ├── Cross over trials in Clinical Research.pdf
│ │ ├── Randomised Response-Adaptive Designs.pdf
│ │ ├── How to Design, Analyse and Report Cluster Randomised Trials in Medicine and Health Related Research.pdf
│ │ ├── Design and Analysis of Cross-Over Trials, Third Edition.pdf
│ │ ├── The Theory of Response-Adaptive Randomization in Clinical Trials (Wiley Series in Probability and Statistics).pdf
│ │ ├── Modern_adaptive_randomized_clinical trial.pdf
│ ├── 其他疾病临床试验
│ │ ├── Clinical Trials in Rheumatology.pdf
│ │ ├── Handbook for Clinical Trials of Imaging and Image-Guided Interventions.pdf
│ │ ├── Clinical Trials in the Neurosciences (Frontiers of Neurology and Neuroscience).pdf
│ │ ├── The CAPRISA Clinical Trials_ HIV Treatment and Prevention.pdf
│ │ ├── Clinical Trials in Osteoporosis.pdf
│ │ ├── Clinical trials in neurology _ design, conduct, analysis.pdf
│ │ ├── Investigative Electrocardiography in Epidemiological Studies and Clinical Trials.pdf
│ │ ├── Clinical Trials in Psychopharmacolog.pdf
│ │ ├── Clinical trials in older people.pdf
│ │ ├── Medical Imaging in Clinical Trials.pdf
│ │ ├── Clinical trials in psychiatry.pdf
│ │ ├── Statistics_in_Clinical_Vaccine trials.pdf
│ │ ├── Success in Academic Surgery_ Clinical Trials.pdf
│ │ ├── Antiviral Drugs_ From Basic Discovery Through Clinical Trials.pdf
│ │ ├── Clinical Trials of Antidepressants_ How Changing the Model Can Uncover New, More Effective Molecules.pdf
│ │ ├── Clinical Trial Design Challenges in Mood Disorders.pdf
│ │ ├── Cardiovascular Clinical Trials_ Putting the Evidence into Practice.pdf
│ │ ├── Global Clinical Trials for Alzheimer's Disease. Design, Implementation, and Standardization.pdf
│ ├── 超全Protocol写作攻略.docx
│ ├── 临床研究Protocol从哪里找.doc
│ ├── 临床试验研究方案的基本内容.doc
│ ├── protocol入门.docx
│ ├── 要点临床试验方案撰写设计思路.doc
│ ├── 收好这份 Protocol，你就是鉴鼠专家.docx
│ ├── Protocol集中营，你值得拥有！.docx
│ ├── 实验Protocol的权威来源网站.docx
│ ├── Study protocol.doc
│ ├── 在临床不会基础研究？这几个网站帮你搞定 protocol.docx
├── 临床试验纳入标准
│ ├── 超强总结！一文带你搞懂 4 种临床试验纳入标准.docx
通过网盘分享的文件下载链接.docx
(13.65 KB, 需要: RMB 29 元)
京公网安备 11010802022788号
