E-Clinical

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eClinical is a term used within the biopharmaceutical industry to refer to electronic systems for automating the management or conduct of clinical trials with the aim of replacing manual, ad hoc or paper-driven methods. Originally, ""eClinical"" was used to refer to any technology application in use within a clinical trial. Without a more specific definition, the industry used ""eClinical"" interchangeably to refer to number of different technologies, such as EDC solutions (Electronic Data Capture), CTMS (Clinical Trials Management System) or Randomization and Trial Supply Management systems, commonly using IVRS (Interactive Voice Response Systems), electronic patient diaries and other common types of electronic solutions widely used in clinical trials.

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The information in this book can show you how to be an expert in the field of E-Clinical.

Are you looking to learn more about E-Clinical? You're about to discover the most spectacular gold mine of E-Clinical materials ever created, this book is a unique collection to help you become a master of E-Clinical.

This book is your ultimate resource for E-Clinical. Here you will find the most up-to-date information, analysis, background and everything you need to know.

In easy to read chapters, with extensive references and links to get you to know all there is to know about E-Clinical right away. A quick look inside: EClinical trial technology, Accelrys, Case report form, ClearTrial, Clinical data acquisition, Clinical Data Interchange Standards Consortium, Clinical data management, Clinical data management system, Clinical Trial Management System, ClinLife, Common Technical Document, Data clarification form, Electronic Common Technical Document, Electronic patient-reported outcome, EudraCT, Mpro, Patient diary, Patient-reported outcome, Source document, Clinical trial, A1chieve, Age-Related Eye Disease Study, ALMANAC, Analysis of clinical trials, Assay sensitivity, ASTEROID trial, AURORA trial, Biological plausibility, British Doctors Study, CapOpus, CDR Computerized Assessment System, Censoring (clinical trials), Clinical significance, Clinical trial effect, Clinical trial protocol, Confirmatory trial, Consolidated Standards of Reporting Trials, Data confidentiality in clinical trials, Dose-ranging study, Dublin Molecular Medicine Centre, End point of clinical trials, European Clinical Research Infrastructures Network, European Forum for Good Clinical Practice, Jesse Gelsinger, Guatemala syphilis experiment, H5N1 clinical trials, Heart Protection Study, IFPMA Clinical Trials Portal, Imaging biomarker, INIT II, Intention to treat analysis, Interim analysis, International Studies of Infarct Survival, Intersalt study, Investigator's brochure, Jadad scale, JUPITER trial, Kano trovafloxacin trial litigation, Length time bias, Medical experimentation in Africa, MIDAS Trial, N of 1 trial, Natural history group, Patient recruitment, Per-protocol analysis, Potentially all pairwise rankings of all possible alternatives, Rule of three (medicine), Scandinavian Simvastatin Survival Study, SDTM...and Much, Much More!

This book explains in-depth the real drivers and workings of E-Clinical. It reduces the risk of your technology, time and resources investment decisions by enabling you to compare your understanding of E-Clinical with the objectivity of experienced professionals - Grab your copy now, while you still can.