AstraZeneca Invests in Data, Discovery Management


By Allison Proffitt

July 14, 2008 | AstraZeneca Discovery’s ten worldwide sites were drowning in information. Scientists had no way to access relevant data; they didn’t even know whether relevant data existed,  whether a test for a particular activity existed, or if a scientists at another site was currently making and testing similar compounds. The solution was IBIS, a system to standardize screening data globally and make it available to AstraZeneca sites by the end of 2006. It was an ambitious goal, but IBIS has saved over 136,000 man hours per year and earned the company a Best Practices award for Knowledge Management. (see Best Practices )

“I think it’s brought a step change in the way we can work with Discovery, because we’ve been able to deliver a system and a project that our customers have agreed has been a real success,” says Nick Lynch, chemistry domain architect for AstraZeneca and technical architect for the program since its inception in 2002. 

The IBIS team came to include over 80 contributors across AstraZeneca. “It was a joint project really,” says Lynch. “With it being distributed over ten sites we had to work really effectively across multiple time zones and multiple sites.”

IBIS, or International Bioscience Information System, is made up of four key components: IBIS Rules, screening data standards; IBIS Test Service that creates and manages test definitions; IBIS Upload, a diagnostic warehouse of more than 150 million screening results; and IBIS Explore, a state-of-the-art query tool.

IBIS Rules, created and managed by a Curation Group, is the backbone of the program and serves as the global standard specifying terminology, business rules, metadata, and vocabularies. These rules provide the means to communicate and process data across the boundaries of sites, projects, and teams. “People talk about IBIS or the IBIS rules in a very positive way,” says Lynch, “and the discovery scientists’ contribution to the rules and their energy to keep them up to date or to govern them in the right way has really been the success.”

 The IBIS Test Service, Explore, and Upload components are all integrated software components developed by Discovery Information and designed to define, capture, validate, distribute, search, and exploit Discovery project data on a global level. “The majority of the [IBIS] code is code we have written,” Lynch says, though he says the team took advantage of open source where they could and use Spotfire and Oracle solutions.

As is almost always the case, AstraZeneca had to weigh the options between buying and building what they needed. The decision came down to ROI, says Lynch. “We felt that we spent a lot of time on building the rules and building our model, and we looked at the commercial tools and we didn’t feel that they could implement rules in the way that we wanted them... So we decided it was more efficient for us to write it.” Lynch estimates that of the total cost of IBIS implementation, only about a third can be attributed to pure IT costs.

IBIS has been fully operational with legacy systems shut off for about 18 months and since then the software tools have been constantly refined, especially around IBIS Explore, as users work with the system and input their data. Lynch says that he and his team have used the IBIS buzz from the Best Practices award to make the case for securing a capability around IBIS to further develop it.

“We’re intending it to be a foundation for our information management and exploitation for a while,” he says. “IBIS is part about the data and part about the actual tools themselves. The data, we spent a lot of effort getting it in a better shape. That can live on independently from this particular version of the tool; it can evolve and grow as we need to.”  

___________________________________________________

This article appeared in Bio-IT World Magazine.

Subscriptions are free for qualifying individuals.  Apply Today.

 

 

 

Click here to login and leave a comment.  

0 Comments

Add Comment

Text Only 2000 character limit

Page 1 of 1

White Papers & Special Reports

waters integrated
Integrated Software Approach to Streamline Method Development Workflow
Sponsored by Waters
Traditional chromatography method development evaluates numerous chromatographic variables that may include selection of the column, solvent, flow rate, etc. This application note demonstrates an integrated approach to capturing and storing separation related reports during chromatography method development.


HP white paper image
Extreme Storage Knowledge Center
Sponsored by HP

Visit HP’s Extreme Storage Knowledge Center to find informative, complimentary white papers, case studies, videos, product information and more.  Brief overview of topics:

  • The challenges of unstructured storage and how to manage both cost-effectively and efficiently
  • Company case studies of data storage challenges that translate across pharmaceutical and biotech companies today
  • Systems that manage vast amounts of data with simple deployment, unified management, and extreme scalability at an exceptionally low price per terabyte
  • Life sciences data management; viable solutions for small and large companies to manage growing storage demands
  • Take our virtual product tour and see our storage unit from inside out


Coupa white paper 92
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:
1) “The ostrich” - Preserve the status quo/hope for the best
2) “The bull in the china shop” - Blindly cut expenses across the board
3) “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.



Life Science Webcasts & Podcasts

Medidata Solutions

Rising Clinical Trial Delays and Costs - Addressing the Cause, Not the Symptoms 

medidata podcastProtocol complexity is taking a toll on clinical study speed and efficiency: increasingly complicated and ambitious protocols are not only burdening sites and study volunteers but are also prolonging trials and increasing expenses. In response, sponsors have turned to global study placement, restructured site relationships and new site management practices, but the problem remains.

This podcast will discuss:

  • Why these responses address only the symptoms, not the underlying cause, of rising clinical trial delays and costs.
  • Results of a recent joint Tufts University / Medidata Solutions study.
  • New metrics benchmarking protocol design trends.
  • Systematic protocol design improvements and why they are essential to clinical trial performance excellence.

Speakers: Ken Getz, Senior Research Fellow at the Tufts Center for the Study of Drug Development, and Ed Seguine, General Manager, Trial Planning Solutions at Medidata.

Download Now 



More Podcasts

Job Openings

Manager, Scientific Computing & Programming
Lead SAIC-Frederick, Inc.’s Bioinformatics & Analysis Group in developing & maintaining informatics pipelines for generation/analysis of dense genotyping & next-generation sequencing data. Required:  MS or equiv.  5 yrs related experience.  Knowledge of programming/software development, high performance computing, bioinformatics, project management. Visit www.saic-frederick.com - #130019.

For reprints and/or copyright permission, please contact The YGS Group, 1808 Colonial Village Lane, Lancaster, PA;

(717) 399-1900 ext. 125, or via email to Ashley.Zander@theYGSgroup.com.