Monday, May 20, 2013

FDA suggests guidelines for expanded access to experimental drugs

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May 20, 2013
Over 1,300 leaders in biofuels, biobased products and renewable chemicals will be in Montreal June 16-19 for the 10th Annual BIO World Congress on Industrial Biotechnology. View the list of attending companies and register now.

The news summaries appearing in BIO SmartBrief are based on original information from news organizations and are produced by SmartBrief, Inc., an independent e-mail newsletter publisher. The information is not compiled or summarized by BIO. Questions and comments should be directed to SmartBrief at bio@smartbrief.com.

  Today's Top Story 
  Health Care & Policy 
  • Alethia wins patent for targeted antibodies to treat cancer
    Alethia Biotherapeutics was granted a U.S. patent for a cancer-treatment method that involves the use of antibodies targeting secreted clusters that play a role in epithelial-to-mesenchymal transition, a key mechanism in tumor invasion and metastasis. "The issuance of this patent broadens our intellectual property estate for the treatment of solid tumors in which sCLU induces EMT," company President and CEO Yves Cornellier said. Pharmaceutical Business Review Online (5/17) LinkedInFacebookTwitterEmail this Story
  • Researchers grow human thymus tissue using stem cells
    Researchers from the University of California at San Francisco grew functioning human thymus tissue using stem cells and growth factors. Thymus tissue plays an important role in the immune system by fostering the growth of T cells. The technique has potential applications in the transplantation of stem cells, tissue and organs, according to the study in the journal Cell Stem Cell. MedicalDaily.com (5/16) LinkedInFacebookTwitterEmail this Story
  Company & Financial News 
  Featured Content 
 

  Food & Agriculture 
 
  • Compulsory biotech labeling would mislead consumers
    Mandatory labeling of biotech foods would only lead consumers to believe there is something wrong with the products, contrary to scientific findings that biotech foods pose no health risks, Harvard Law School professor Cass R. Sunstein writes. "Unless science can identify a legitimate concern about risks to health or the environment, the argument for compulsory GM labels rests on weak foundations," Sunstein argues. Staten Island Advance (N.Y.)/Bloomberg (5/19) LinkedInFacebookTwitterEmail this Story
 
Webcast: A Conversation with The Johns Hopkins Hospital on Lowering the Cost of Healthcare from Inside Out
Learn how The Johns Hopkins Hospital uses its Integrated Asset and Service Management solution to improve uptime to support patient care; control costs for procurement, maintenance, labor and materials; support regulatory compliance activities; and use workflow capabilities for internal controls. Watch the webcast.

  Hot Topics 

Top five news stories selected by BIO SmartBrief readers in the past week.

  • Results based on number of times each story was clicked by readers.
  Industrial & Environmental 
  • Calif. cellulosic ethanol plant achieves operational milestone
    Edeniq's demonstration-scale cellulosic ethanol plant in Visalia, Calif., has reached a milestone by surpassing 1,000 hours of continuous operation. The facility also met the Department of Energy's goal for operational reliability, the company said. The next step for Edeniq is to make further improvements and continue operations at the plant with the California Energy Commission's co-sponsorship. DomesticFuel.com (5/16) LinkedInFacebookTwitterEmail this Story
  News from BIO 
  • Secure document sharing services optimized for life science organizations
    ShareVault, a leading provider of highly secure and controlled document sharing solutions and virtual data rooms (VDR), has aligned with BIO to provide companies with significant discounted pricing and complimentary extra features. ShareVault's VDR platform is optimized for life science companies of all sizes and flexibly priced so that even small biotech companies can afford and benefit from its technology. The ShareVault solution is intended for due diligence required during bio-pharma partnering, licensing, fundraising, M&A, clinical study management or other applications that require secure sharing of documents with third parties. Learn more and sign up for a free trial. LinkedInFacebookTwitterEmail this Story
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  SmartQuote 
I regret nothing, says arrogance; I will regret nothing, says inexperience."
--Marie von Ebner-Eschenbach,
Austrian writer


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