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eCliniqua - Innovative Management in Clinical Trials
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A Bio-IT World publication
Monday, January 05, 2009 |  Bio-ITWorld.com | Archives | Advertising | Your Account | CHI Conferences | Subscribe |

Industry Trends

Protocol Design Impact on Patient Recruitment and Retention Rates
1999-02 vs. 2003-06

By Mark P. Mathieu

Enrollment rates for volunteers who met the rising number of protocol eligibility criteria dropped from 75% in 1999-02 to 59% in 2003-06.
Read more

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Kay O. Christopher
eCliniqua Specialist
860-693-2991 office
857-636-0934 cell
 

Contact the editors 

   
Contributing Editor Deborah Borfitz covers development planning and protocol design; investigative site selection and management; and patient recruitment and retention.

  
Contributing Editor Ann Neuer covers project management, operations, and outsourcing, as well as data collection, data management, and electronic data capture. Ann has been writing in the clinical trials sector since 1995.

Managing Editor Allison Proffitt manages and produces eCliniqua.

Link to Us! 
You are welcome to link to articles on our website. Contact Allison Proffitt for details.

e-Prints & Reprints 
To post a full article from eCliniqua or Bio-IT World on your website (not just a link), or for paper reprints, please contact:
Ashley Zander

The YGS Group
717-399-1900 ext.125

IN THIS ISSUE 
caBIG: Fostering Better Connections with Open Source Software 
Kevin Davies Sits Down With Paul Bleicher 
Workgroup Sets Priorities to Harmonize Standards for EHRs and Research 
NIH Takes Clinical Research Course Directly to Beijing
 
  
 

OPEN SOURCE
caBIG: Fostering Better Connections with Open Source Software
By Deborah Borfitz

The free, open source clinical trials software tools of the cancer Biomedical Informatics Grid (caBIG) have been downloadable, in a single bundle, from the website of the National Cancer Institute (NCI) Center for Biomedical Informatics and Information Technology since early last year. With November’s release of the caBIG Clinical Trials Suite (version 1.1), individual components also have newfound speed and simplicity of use.

The Suite, overall, can be more easily configured and installed and has enhanced user interfaces and documentation, says John Speakman, associate director of clinical trials products and programs for the Center. While the software has been crafted in response to the needs of clinical researchers in oncology, it is “by and large generic” and thus widely applicable beyond cancer. More.

 
 

WEBCAST
Kevin Davies Sits Down With Paul Bleicher


 

 

STANDARDS
Workgroup Sets Priorities to Harmonize Standards for EHRs and Research
By Ann Neuer

The much anticipated convergence of data between clinical trials and electronic health records (EHR) is heading toward reality with the recent formation of the EHR Clinical Research Value Case Workgroup. Convened in November by the American National Standards Institute (ANSI), the workgroup is a cross-section of experts from industry, academia, standards organizations, and government who have come together to identify priorities for the harmonization of technical standards needed to ensure the interoperability of EHRs and global clinical research applications.

“It’s a neutral group of stakeholder representatives that will set priorities for interoperability specification development in the clinical research space,” says Rebecca Kush, president and CEO of the Clinical Data Interchange Standards Consortium (CDISC) and co-chair of this initiative. More.

 

TRAINING
NIH Takes Clinical Research Course Directly to Beijing
By Deborah Borfitz

The National Institutes of Health (NIH) recently debuted an introductory course on the principles and practice of clinical research in Beijing, China. The course is normally taught over one semester at the Clinical Center, the NIH’s clinical research hospital in Bethesda, says director John Gallin. But last November, 111 physicians completed the same course in Beijing, compressed into one week, and did as well on their final as students taking the class’s longer version. More. 

 
 

Most-Read Story from Previous Issue
2009 Clinical Trials Predictions and Resolutions 

 
 
 
 

FEATURED EVENTS

The Association for Laboratory Automation (ALA) presents LabAutomation2009, January 24-28, in Palm Springs, CA. 

Immunogenicity for Biotechnology - January 26-27,2009

Health 3.0: Next Online Generation - January 26-28,2009 

Meeting the Challenges of Global Clinical Supply Chain Management,
 January 27th, 2009 

The BIO IT Coalition -
 
January 28, 2009 

Electronic Laboratory Notebooks - 28th - 29th, January 2009, Copthorne Tara Hotel, London, United Kingdom

TEPR+ 2009 - Feb 1-5, 2009 | Palm Springs, CA

You May Not Know What You Don't Know About Managing Your Trials, February 5th, 2009 

The World Health Care Congress 2nd Annual Leadership Summit on Consumer Connectivity & Web Empowerment | February 23 – 24, 2009-
Carlsbad, CA 

ABRF- 2009/Application and Optimization of Existing and Emerging Biotechnologies -  February 7-10, 2009

16th International Molecular Medicine Tri-Conference -February 25-27, 2009 

Electronic Data in Clinical Trials  March 11-12, 2009 – 
Miami, FL 

BIO IT Coalition's 8th annual Conference -
 
April 22, 2009 

Bio-IT World Conference & Expo – April 27-29, 2009  

Barnett Educational Services

Cambridge Healthtech Events

To have your event featured here, contact Lynn Cloonan for more information.

 
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Bio-IT World's 2009 Best Practices Awards Program

Entry forms are now available for Bio-IT World’s 2009 Best Practices Awards program. The program is intended to spotlight companies whose use of innovative technologies is making a positive difference in biomedical R&D and drug discovery and development.

Bio-IT World is also making available a free compendium of Best Practice entries from 2008 to help ensure the lessons learned are widely spread. The compendium can be downloaded here.

Full details of the entry process and the entry form are available by clicking here. The deadline is mid-January 2009. 

2009 Best Practice Categories:
*Basic Research & Biological Research
*Drug Discovery & Development
*Clinical Trials & Research
*Translational Medicine
*Personalized Medicine
*IT & Informatics
*Knowledge Management
*Health-IT
*Manufacturing & Bioprocessing

If you have questions, write to aproffitt@healthtech.com

FEATURED CONTENT

High-Performance Computing in Life Science & Education, underwritten by SGI and Intel 

The varied collection of Bio-IT World articles and insights assembled in this BriefingON examine key trends in HPC infrastructure and how researchers are putting their best computational resources to use. Provided here are stories and lessons around the effective use of high performance computing in life science. Download the BriefingON.   

10 Secrets to Recession-Proof Your Business
Sponsored by Coupa

Read this white paper to discover 10 strategies smart companies deploy to recession-proof their business.
Leaders generally face hard choices on how to mange a company during an economic downturn and
behave in one of three ways:
• “The ostrich” - Preserve the status quo/hope for the best
• “The bull in the china shop” - Blindly cut expenses across the board
• “The fox” - Use the downturn to make your business more effective and position it for future growth.
Learn how to behave “like a fox” and use a recession as a means to pounce on emerging trends.
Download This Complimentary Paper.

Next Generation Sequencing  Learn how labs can maximize the value they receive from their next generation sequencing instruments:
sponsored by Genologics

How can labs generate value from their next generation sequencing instruments
What are the data management challenges for labs conducting next generation sequencing
What do genomics labs need to look for when evaluating lab and data management systems
How are different labs using a lab and data management system to address their data management challenges
Download Now 

To have your white paper featured here, contact Lynn Cloonan for more information.

EXCLUSIVE WEBCAST

Life Science Webcasts from Bio-IT World and Cambridge Healthtech Media Group

Life Science Webcasts

NEW!
Exploring Next-Generation Sequencing
Bio-IT World Editor-in-Chief Kevin Davies interviews BGI’s Laurie Goodman on the sequencing of the first Asian genome. View the webcast.

Drug Discovery, Development and Commercialization: Evolving Challenges and Opportunities
Joshua Boger, PhD, president and CEO, Vertex Pharmaceuticals Inc., delivers his keynote at the 2008 Bio-IT World Conference & Expo in Boston, April 30, 2008.
View the webcast.

Personalized Genetics: Advancements and Driving Change
Linda Avey, co-founder of 23andMe, delivers her keynote at the 2008 Bio-IT World Conference & Expo in Boston, April 30, 2008.
View the webcast.

The Future of Personal Genomics
A distinguished panel of personal genomics experts discuss the future of personal genomics at the 2008 Bio-IT World Conference & Expo in Boston, April 30, 2008.  They include Dietrich Stephan (co-founder, Navigenics); George Church (Harvard Medical School); Jeff Drazen (editor-in-chief, New England Journal Medicine); Fred Ledley (Bentley College); John Halamka (CIO, Harvard Medical School); and Linda Avey (23andMe). Bio-IT World Editor-in-Chief Kevin Davies moderates the discussion.
View the webcast.

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                                Healthtech Media GroupPublished by Cambridge Healthtech Media Group, division of CHI, Copyright © 2008; All rights reserved. eCliniqua may not be reproduced, electronically or in print, by any means, mechanical or electronic, in whole or in part, without written permission of Cambridge Healthtech Media Group, 250 First Ave., Suite 300, Needham, MA, 02494. 
For reprints and/or copyright permission, please contact The YGS Group, 1808 Colonial Village Lane, Lancaster, PA 17601.  Phone: 717-399-1900, ext. 125. Email: ashley.zander@theYGSgroup.com