Industry Trends

Clinical Research
Off-shoring: A Country Attractiveness Index for Clinical Trials

By Mark P. Mathieu
For many years, pharmaceutical companies have been off-shoring manufacturing operations to lower-cost countries. Healthy margins and strong risk aversion have afforded pharmaceutical companies the luxury of staying close to home, for all but manufacturing activities. As financial pressures increase, pharmaceutical executives are finding that going offshore is not only less risky than it once was, but also too attractive to ignore.  Read More




IBM’s Sunny Forecast for Clinical Cloud Computing



By Deb Borfitz

June 1, 2009 | An increasing number of the top life science companies are considering a switch from the outright acquisition and customization of e-clinical technologies to establishing and accessing “clinical clouds.” Indeed, it may be the only sensible way to access needed software and information as they engage in more collaborations, alliances, and partnerships to weather the “perfect storm of unprecedented challenges” bearing down on their collective bottom line, says Paul Papas, the Americas life sciences leader for IBM Global Business Services.

Paul_Papas
Paul Papas
Historically, most large pharmaceutical firms have run fully integrated vertical business models, doing all they can in-house and “choosing to selectively outsource where appropriate,” says Stuart Henderson, IBM’s Americas life sciences research and development leader. But many are moving to a network business model where they share risks, rewards, financing, and resources with a portfolio of partners to, among other things, develop and commercialize drugs. As companies do less within their four walls and seek to reduce the time and cost of clinical development, the demand for hosted, fully integrated, end-to-end clinical solutions will rise because sharing an integrated platform is cheaper, less time consuming, and more supportive of a networked business model than the alternative.

The enabler of all this is cloud computing, an Internet-based model wherein a broad range of applications can be tapped from just about anywhere. Users needn’t know anything about the technology infrastructure in the cloud that supports them. They pay cloud computing service providers like IBM and Amazon only for the resources they need and use.

“Building a smarter clinical cloud will enable collaboration, transparency, and access to real-time information wherever it is created,” says Papas. According to IBM, a “smarter” clinical cloud consists of ten core capabilities: multi-tenant security, file sharing, data sharing, help and support, collaboration, analytics, compliance, clinical application suite, process integration and orchestration, and infrastructure.

Clinical cloud computing is certainly more economical for companies than buying  licenses for separate electronic data capture (EDC), clinical trial management (CTM), and information management systems, integrating them internally, and then redundantly paying for the same services whenever they use a clinical research organization, says Henderson.

The FDA already trusts external servers when clinical trial data is sent by email from labs to investigators and from investigators to sponsors, says FDA spokesperson Crystal Rice. But if the data is archived using cloud computing, sponsors will have to convince the agency that there are adequate “write protection” safeguards to prevent tampering. The FDA would be particularly interested in data security measures if the cloud computing service provider has other “sensitive users” such as insurance companies and banks. “The agency might [also want to] check for assurance that investigator records correspond with the data in the cloud repository.”

IBM predicts that life science companies will “flip” to buying technology in a cloud-provisioned way within no more than three to five years. “The situation will be less about which products they use to do EDC or CTM,” says Papas. “The majority of talented clinical IT resources now focused on operational efforts will instead be focused on the science of analytics.”

So what will companies do with the millions of dollars of technology they have already invested in? “There are multiple options and much depends on the investment lifecycle for each clinical application for each client,” says Papas. “IBM’s approach is to enable a phasing to cloud computing where a client uses a combination of their in-house applications and the applications available as part of the cloud solution.”

The move to cloud computing will essentially force companies to agree not just on how they will collect and exchange clinical data, but also how they will manage and warehouse it, says Henderson. “What companies increasingly agree on is that the differentiation they bring is not in the applications they use to execute studies, but the study design, the assets being progressed through the pipeline, and their relationships with clinical investigators.”

When done right, Papas says, a clinical cloud will facilitate company-specific variations via configuration rather than customization. “Companies will have to realize and accept that most customizations are costly and do not provide differentiation.”

Click here to log in.

0 Comments

Add Comment

Text Only 2000 character limit

Page 1 of 1

White Papers & Special Reports

Life Science Webcasts & Podcasts

medidata podcast #8 Meeting Today’s Challenges in Clinical Trial Supply Management
Sponsored by: Medidata Solutions Worldwide  

Setting up and managing the clinical trial involves many complex procedures. Among the most challenging are planning and executing the logistics of the trial’s clinical supplies. This podcast focuses in depth on the following topics which trace current practices and future evolution of this crucial aspect of clinical trials:

  • Current practices in clinical trial logistics
  • Comparing advances in clinical supply practices to  other aspects of clinical trials 
  • Where current practices fall short of meeting the challenges
  • Trends and evolving improvements that may change the way logistics are conducted

Listen Now  


More Podcasts

Job Openings

tessella logo 
Scientific Software Engineer
Boston MA
$70,000 to $95,000
 

Tessella delivers software engineering and consulting services to leading pharmaceutical and biotech companies. We are recruiting Software Engineersto work with skilled bioinformaticians and scientists to identify business needs and recommend and develop technical solutions. Applicants require BS, MS or PhD in bioinformatics, biology or chemistry and 2+ years of software development in either: Java, C#, C++, C or VB.NET. 

Apply at http://jobs.tessella.com   

 

oxford nanopore logo 


 Early Access Collaborations Managers
Oxford Nanopore Technologies is developing a novel technology, GridIONTM for the direct, electronic analysis of DNA/RNA and other analytes.  As the system approaches the market, we are building a team of technically knowledgeable, highly motivated candidates with excellent customer service and facilitation skills to join our company as Collaboration Managers.  This is a unique opportunity to work with world-leading genomics customers throughout the early adoption phase of a new generation of DNA sequencing technology.. This is a facilitative, enabling role with responsibility for managing technology development collaborations with key customers at leading genomics institutions.  It will include long term management of the collaboration plan and milestones and associated meetings and documentation. Click here to find out more and apply   

Oxford Nanopore's GridION technology, VP, Sales and Marketing Oxford Nanopore Technologies is a fast-moving technology company that is developing a novel electronic molecular analysis technology. The technology is adaptable for the analysis of DNA/RNA, proteins, chemicals and other molecules.  It is therefore suitable for use in a variety of markets including scientific research and clinical applications.  As the technology approaches the market, Oxford Nanopore is seeking a visionary VP of sales and marketing to join the senior team.  The candidate will embrace the opportunities afforded by entering the market with a truly disruptive technology that has the potential to expand the number of users and the variety of applications in each target market.  This is a rare opportunity to influence the commercial strategy at an early phase of its commercial lifetime, in a well funded company.  Oxford Nanopore welcomes applications from candidates with a track record of high-level strategic commercial  leadership, who wish to apply a fresh approach to existing markets.  Experience in Life Sciences/DNA sequencing is central to this role, however we will consider your application if you have experience of disruptive technologies in other related industries.  We are particularly interested in candidates with strong expertise in the use of digital technologies for sales and marketing of scientific/technical products.  Click to  Apply  


 





Sponsored Links

For reprints and/or copyright permission, please contact  Tim McLucas, (781) 972-1342, tmclucas@healthtech.com .