Eclinical Trials

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Eclinical Trials

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Author : Rebecca Daniels Kush
language : en
Publisher: CenterWatch
Release Date : 2003

Eclinical Trials written by Rebecca Daniels Kush and has been published by CenterWatch this book supported file pdf, txt, epub, kindle and other format this book has been release on 2003 with Medical categories.

Eclinical Trials

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Author :
language : en
Publisher:
Release Date : 2010

Eclinical Trials written by and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2010 with categories.

Pharmaceutical Eclinical Trials Outsourcing

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Author : MaryAnne F. Rizk
language : en
Publisher:
Release Date : 2012

Pharmaceutical Eclinical Trials Outsourcing written by MaryAnne F. Rizk and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2012 with Drugs categories.

E Clinical High Impact Strategies What You Need To Know

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Author : Kevin Roebuck
language : en
Publisher: Tebbo
Release Date : 2011

E Clinical High Impact Strategies What You Need To Know written by Kevin Roebuck and has been published by Tebbo this book supported file pdf, txt, epub, kindle and other format this book has been release on 2011 with Computers categories.

The Knowledge Solution. Stop Searching, Stand Out and Pay Off. The #1 ALL ENCOMPASSING Guide to E-Clinical. An Important Message for ANYONE who wants to learn about E-Clinical Quickly and Easily... ""Here's Your Chance To Skip The Struggle and Master E-Clinical, With the Least Amount of Effort, In 2 Days Or Less..."" 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. Get the edge, learn EVERYTHING you need to know about E-Clinical, and ace any discussion, proposal and implementation with the ultimate book - guaranteed to give you the education that you need, faster than you ever dreamed possible! 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.

Re Engineering Clinical Trials

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Author : Peter Schueler
language : en
Publisher: Academic Press
Release Date : 2014-12-16

Re Engineering Clinical Trials written by Peter Schueler and has been published by Academic Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2014-12-16 with Medical categories.

The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Engineering Clinical Trials evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and offers you well-established methodologies and best practices based on real-world experiences from expert authors across industry and academia. Written for all those involved in clinical research, development and clinical trial design, this book provides a unique and valuable resource for streamlining the process, containing costs and increasing drug safety and effectiveness. Highlights the latest paradigm-shifts and innovation advances in clinical research Offers easy-to-find best practice sections, lists of current literature and resources for further reading and useful solutions to day-to-day problems in current drug development Discusses important topics such as safety profiling, data mining, site monitoring, change management, increasing development costs, key performance indicators and much more

Drug Discovery And Clinical Research

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Author : SK Gupta
language : en
Publisher: JP Medical Ltd
Release Date : 2011-06

Drug Discovery And Clinical Research written by SK Gupta and has been published by JP Medical Ltd this book supported file pdf, txt, epub, kindle and other format this book has been release on 2011-06 with Medical categories.

The Drug Discovery and Clinical Research bandwagon has been joined by scientists and researchers from all fields including basic sciences, medical sciences, biophysicists, biotechnologists, statisticians, regulatory officials and many more. The joint effort and contribution from all is translating into the fast development of this multi-faceted field. At the same time, it has become challenging for all stakeholders to keep abreast with the explosion in information. The race for the finish-line leaves very little time for the researchers to update themselves and keep tabs on the latest developments in the industry. To meet these challenges, this book entitled Drug Discovery and Clinical Research has been compiled. All chapters have been written by stalwarts of the field who have their finger on the pulse of the industry. The aim of the book is to provide succinctly within one cover, an update on all aspects of this wide area. Although each of the chapter dealt here starting from drug discovery and development, clinical development, bioethics, medical devices, pharmacovigilance, data management, safety monitoring, patient recruitment, etc. are topics for full-fledged book in themselves, an effort has been made via this book to provide a bird’s eye view to readers and help them to keep abreast with the latest development despite constraints of time. It is hoped that the book will contribute to the growth of readers, which should translate into drug discovery and clinical research industry’s growth.

The Flexible Enterprise

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Author : Sushil
language : en
Publisher: Springer Science & Business Media
Release Date : 2013-11-19

The Flexible Enterprise written by Sushil and has been published by Springer Science & Business Media this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-11-19 with Business & Economics categories.

The need for enterprise flexibility in an era of rapidly advancing technology, increasing competition, and globalization, is apparent. Flexibility can be thought of as an ability of the enterprise to quickly and efficiently respond to market changes and to bring new products and services quickly to the market place. Beyond this definition, a truly flexible enterprise should proactively change the market through its ability to create new and innovative products and services. The proposed book is intended to provide a conceptual framework of ‘Flexible Enterprise’ supported by researches/case applications in various types of flexibilities exhibited by a flexible enterprise. The selected papers from a variety of issues concerning the planning and operation of a flexible enterprise are organized into following four parts: I Enterprise and Strategic Flexibility II Organizational Flexibility III Business Process and Information Systems Flexibility IV Operations Flexibility

Innovation In Clinical Trial Methodologies

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Author : Peter Schueler
language : en
Publisher: Academic Press
Release Date : 2020-11-01

Innovation In Clinical Trial Methodologies written by Peter Schueler and has been published by Academic Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2020-11-01 with Medical categories.

Innovation in Clinical Trial Methodologies: Lessons Learned during the Corona Pandemic presents a selection of updated chapters from Re-Engineering Clinical Trials that feature innovative options and methods in clinical trials. The Coronavirus pandemic is an accelerator for digitalization in many industries, including clinical trials. This book considers best practices, alternative study concepts requiring fewer patients, studies with less patient interaction, the design of "virtualized" protocols, and moving from data to decisions. This book will be helpful to pharmacologists, physicians and clinical researchers involved in the process of clinical development and clinical trial design. Considers multiple digital and virtual strategies Explores best practices, including the use of reduced patient involvement Brings together expert, trusted information to increase the efficiency and effectiveness of clinical trials

National Institute Of Dental Research Annual Report

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Author : National Institute of Dental Research (U.S.)
language : en
Publisher:
Release Date : 1976

National Institute Of Dental Research Annual Report written by National Institute of Dental Research (U.S.) and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1976 with Dentistry categories.

A Manager S Guide To The Design And Conduct Of Clinical Trials

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Author : Phillip I. Good
language : en
Publisher: John Wiley & Sons
Release Date : 2006-04-21

A Manager S Guide To The Design And Conduct Of Clinical Trials written by Phillip I. Good and has been published by John Wiley & Sons this book supported file pdf, txt, epub, kindle and other format this book has been release on 2006-04-21 with Mathematics categories.

This newly updated edition of the benchmark guide to computer-assisted clinical trials provides a comprehensive primer for prospective managers. It covers every critical issue of the design and conduct of clinical trials, including study design, organization, regulatory agency liaison, data collection and analysis, as well as recruitment, software, monitoring, and reporting. Keeping the same user-friendly format as the original, this Second Edition features new examples and the latest developments in regulatory guidelines, such as e-submission procedures and computerized direct data acquisition. The new edition also reflects the increasing globalization of clinical trial activities, and includes new information about international standards and procedures, including the Common Technical Document and CDISC standards. This step-by-step guide is supported by handy checklists and extracts from submitted protocols. Experienced author and consultant Phillip Good incorporateshumorous yet instructive anecdotes to illustrate common pitfalls. Based on the proven industrial formula of planning, implementing, and finally performing essential checks, the book's three sections-"Plan," "Do," and "Check"-includethe following material: * Should the trials be conducted? * Put it in the computer and keep it there * Staffing for success * Designing trials and determining sample size * Budgeting * Recruiting and retaining patients and physicians * Data management * Monitoring the trials * Data analysis * After action review * Exception handling Executive and managerial professionals involved in the design and analysis of clinical experiments, along with clinical research associates, biostatisticians, and students in public health will find A Manager's Guide an indispensable resource. Praise for the First Edition: ". . . readable, informative and at times witty . . . never stops being concise and well written . . . a book worth a read . . ." -Statistics in Medicine "The book is very prescriptive and full of lists and tables with which to guide managers in making effective decisions in using computer-assisted clinical trials in pharmaceutical studies." -Technometrics "This book is must-have reading for anyone in the business . . ." -Clinical Chemistry