February 9, 2010
| Bio-IT World > eClinical Trials
eClinical Trials

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Tailored Treatments Require New Trial Design Rules

Aug 4, 2009 | When the clinical feasibility of molecular targeted agents (MTAs) is being tested, “faster answers” will require better use of creative trial designs and approaches, says Timothy Yeatman, president and CSO of M2Gen.

At DIA, India Showcases Growing Clinical Trials Capability

Aug 4, 2009 | India staged a major presence at the recent DIA Annual Meeting in San Diego. From the India Pavilion in the Exhibit Hall to dedicated sessions to a special “India evening”, it was clear that India is positioning itself to be a major player.

Boosting Adaptive Clinical Trials

Bio-IT World | Best Practices | Wyeth Research and partners are developing trial simulation software to streamline the process of designing and running adaptive clinical trials (ACTs). 

Lilly: Innovation and Drug Delivery Technology

eCliniqua | William Heath, vice president of product research and development at Eli Lilly and Company, talked to eCliniqua about the rise in clinical trial activity around new modes of drug delivery.

Will Regulated Product Submission (RPS) Trump eCTD?

eCliniqua | Just as the electronic common technical document (eCTD) is gaining traction as the required format for electronic regulatory submissions, the Food and Drug Administration (FDA) is changing the game. FDA is planning to implement an agency-wide standard known as Regulated Product Submission (RPS) that is expected to replace eCTD. 

White Papers & Special Reports

Quantum
StorNext 4.0: Technical Product Brief
Sponsored by Quantum

 
Proven in the world’s most data intensive industries, Quantum StorNext is a scalable, high-performance file system which allows data sharing across Linux, Mac, Unix, and Windows operating systems and manages data in enterprise storage environments. In this Technical Brief you'll learn:

  • How a high-performing file system can accelerate your business
  • How to simplify your data management
  • How a tiered storage approach can save you money


SURETY-IP_WPx108
Protect Your Scientific Intellectual Property: Proof of Lab Informatics Data Authenticity is Your Best Legal Defense
Sponsored by Surety, LLC

As a bio-technology or life sciences organization, your formulas, treatments and research and discoveries are the “lifeblood” of your business. But if you aren't protecting the integrity of your scientific data in your lab informatics systems, you risk losing IP ownership, revenue and consequently your business if you can't prove time-of-creation and data authenticity. Learn how you can implement simple, cost-effective and automated controls to protect your scientific intellectual property. Consider:

  • IP protection requirements in bio-pharma and other science-oriented industries can extend out 20, 30, 40 or more years
  • Most electronic lab management solutions include generic authenticity controls, so how "legally defensible" is yours?
  • Only standards-compliant, independent controls can future-proof your approach to long-term IP integrity protection and authenticity.
  • Learn more - get the free whitepaper now


BlueArc_WP_DataMigration.jpg
The Key to Life Sciences Data Management: Transparent Migration
Sponsored by BlueArc

Life sciences organizations face new data management challenges as the volume of research data grows and more data is kept online for longer times. Read this paper to learn about:

  • The benefits of transparent data migration (TDM)
  • How TDM technologies can simplify data management.
  • How using TDM can help increase storage utilization, improve computational workflow performance, and optimize the use of storage resources.


Life Science Webcasts & Podcasts

adobe_i3_btn_webinarNext-Generation Clinical Trial and Data Management Applications
Sponsored by Adobe

This webinar introduces i3Cube - a web-based, fully integrated, clinical trial and data management system built on Adobe’s LiveCycle® Enterprise Suite.  I3 cube provides end-to-end automation that delivers unprecedented visibility into information that sponsors need to accelerate the study process and complete trials efficiently. Viewers will learn more about:

  • Creating faster and more efficient trial processes
  • Reducing investigator burden 
  • Real-time sponsor transparency into study information
  • Enterprise solutions based on Adobe LiveCycle® ES utilizing cross-platform clients of Reader, Flash and AIR

    Download now.



More Podcasts

Job Openings

Employers -- Don't miss this opportunity to reach well-qualified life science candidates.




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