REGISTER FOR TOUCH BRIEFINGS |
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Register for touch briefings
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Touch Briefings welcomes editorial submissions for inclusion within our print reports and website from industry practitioners.
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DATA MANAGEMENT IN PHARMACEUTICAL R&D - OPTIMISING ECLINICAL (ORACLE) |
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Welcome to the PDF book page of Data Management in Pharmaceutical R&D - Optimising eClinical report. In these pages you will find articles from experts who are dealing with the challenges of collecting, storing, analysing and sharing electronic clinical data. They talk about the difficulties of moving from pilot schemes to full-scale roll-outs, and of implementing the new technologies. We hope you enjoy Optimising eClinical.
Contents:
Contents
Foreword
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Embracing New Challenges: Clinical Development – The New Opportunity
Jonathan Palmer1 and Nicholas Giannasi, PhD2
1. Business Development Lead, Clinical Solutions, Europe, Middle East and Africa (EMEA), Oracle, and 2. Senior Business Development Director, Life Sciences, EMEA, Oracle
click here to view ebook
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Introduction
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Putting the ‘e’ in R&D
Michelle Grayson
Managing Editor, Medical Communications, Touch Briefings
click here to view ebook
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Optimising eClinical
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Data Integration – Business Requirements and Implications for Data Standards
Sharon Marmaras
Director, Clinical Trial Support and Life Sciences Data Hub (LSH) Business Project Leader, Boehringer Ingelheim
click here to view ebook
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The Convergence of Healthcare and Clinical Research Standards
Pierre-Yves Lastic, PhD
Senior Director, Standards Management & Data Privacy, sanofi aventis R&D
click here to view ebook
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Scaling Up Clinical Research by Expansion of Electronic Infrastructure
Peter J van der Spek, PhD Professor and Head, Department of Bioinformatics, Erasmus University Medical Centre
click here to view ebook
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Clinical Trials Abroad – ‘Back in the USSR’
Vladimir V Novakovskiy, MD, PhD Vice President of Regulatory Affairs and Quality Assurance, Congenix LLC
click here to view ebook
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