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Why Most Clinical Research Is Not UsefulProject Management of Randomized Clinical Trials: A Narrative ReviewUse of mobile devices and the internet for multimedia informed consent delivery and data entry in a pediatric asthma trial: Study design and rationaleKey cost drivers of pharmaceutical clinical trials in the United StatesInternational health research monitoring: exploring a scientific and a cooperative approach using participatory action researchElectronic health records to facilitate clinical research.Evaluation of Data Entry Errors and Data Changes to an Electronic Data Capture Clinical Trial DatabaseDevelopment and implementation of PROgmatic: A clinical trial management system for pragmatic multi-centre trials, optimised for electronic data capture and patient-reported outcomes.Data fraud in clinical trials.The impact of clinical trial monitoring approaches on data integrity and cost--a review of current literature.Constitutional multicenter bank linked to Sasang constitutional phenotypic data.Comparative costs and activity from a sample of UK clinical trials units.Economic analysis of centralized vs. decentralized electronic data capture in multi-center clinical studiesValidity of an information and communication technology system for data capture in epidemiological studies.Evaluating protocol lifecycle time intervals in HIV/AIDS clinical trials.Electronic versus manual data processing: evaluating the use of electronic health records in out-of-hospital clinical research.A statistical approach to central monitoring of data quality in clinical trials.Clinical trials in crisis: Four simple methodologic fixes.Developing regulatory-compliant electronic case report forms for clinical trials: experience with the demand trial.INVESTIGATING THE EFFICACY OF CLINICAL TRIAL MONITORING STRATEGIES: Design and Implementation of the Cluster Randomized START Monitoring Substudy.Improved responsiveness and reduced sample size requirements of PROMIS physical function scales with item response theory.Preparing for the ICD-10-CM Transition: Automated Methods for Translating ICD Codes in Clinical Phenotype Definitions.Generating evidence on a risk-based monitoring approach in the academic setting - lessons learnedA comparative effectiveness study of eSource used for data capture for a clinical research registry.The impact of data errors on the outcome of randomized clinical trials.Electronic dental record use and clinical information management patterns among practitioner-investigators in The Dental Practice-Based Research Network.The future of monitoring in clinical research - a holistic approach: linking risk-based monitoring with quality management principles.Impact of the Patient-Reported Outcomes Management Information System (PROMIS) upon the design and operation of multi-center clinical trials: a qualitative research study.Lessons learned: Infrastructure development and financial management for large, publicly funded, international trials.Cost-effective recruitment methods for a large randomised trial in people with diabetes: A Study of Cardiovascular Events iN Diabetes (ASCEND).The clinically-integrated randomized trial: proposed novel method for conducting large trials at low cost.mHealth and Application Technology Supporting Clinical Trials: Today's Limitations and Future Perspective of smartRCTs.Bridging the gap: improving clinical development and the regulatory pathways for health products for neglected diseases.A systematic search for reports of site monitoring technique comparisons in clinical trials.A systematic review of on-site monitoring methods for health-care randomised controlled trials.Central site monitoring: results from a test of accuracy in identifying trials and sites failing Food and Drug Administration inspection.Barriers to the conduct of randomised clinical trials within all disease areas.Improving public health by improving clinical trial guidelines and their application.A model for the determination of pollen count using google search queries for patients suffering from allergic rhinitis.Discussion: The role, position, and function of the FDA-The past, present, and future.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Sensible approaches for reducing clinical trial costs.
@en
Sensible approaches for reducing clinical trial costs.
@nl
type
label
Sensible approaches for reducing clinical trial costs.
@en
Sensible approaches for reducing clinical trial costs.
@nl
prefLabel
Sensible approaches for reducing clinical trial costs.
@en
Sensible approaches for reducing clinical trial costs.
@nl
P2093
P2860
P50
P356
P1433
P1476
Sensible approaches for reducing clinical trial costs.
@en
P2093
Beena S Cracknell
Elizabeth D Reid
Eric L Eisenstein
Mary Ann Sellers
Michael L Terrin
Oscar Podesta
Rafael Diaz
Rory Collins
Yuriy Shakhov
P2860
P356
10.1177/1740774507087551
P577
2008-01-01T00:00:00Z