Reading this on a mobile device? Try our optimized mobile version here: http://r.smartbrief.com/resp/sEeghMrCDrpEhhgjaP

November 4, 2009
View the free BIO eNewsletter to see why slowed activity is thought to be temporary as plenty of companies still look to be acquired.

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 
 
Internet-enabled technologies such as electronic data capture have transformed clinical development practices, efficiently supporting faster, larger, and more complex trials. Learn from leaders of organizations in the forefront of the EDC movement about the experiences of working with EDC solutions, and related challenges, successes and lessons learned. Download the report now.
  Health Care & Policy 
  • Patient safety should be addressed in follow-on biologics measure
    Congress should ensure that patient safety and medical efficacy are prioritized in a health reform measure that allows the use of follow-on biologics, Dr. David B. Nash of the Jefferson School of Population Health writes in The Hill. Rather than just debating data exclusivity for FOBs, lawmakers should also specify rules on testing these drugs and consider requiring post-market surveillance to avoid "unintended consequences" that compromise patient safety, Nash writes. The Hill (11/3) LinkedInFacebookTwitterEmail this Story
  • Genetically engineered fruit flies could aid diabetes research
    U.S. scientists modified genes in fruit flies to simulate the inability of Type 1 diabetics to produce insulin. "We can use these genetically manipulated flies as a model to understand defects underlying human diabetes and to identify genes and target points for pharmacological intervention," one of the researchers said. The team also is studying Type 2 diabetes with the flies. United Press International (11/3) LinkedInFacebookTwitterEmail this Story
  • Drug-loaded nanoparticles zero in on tumors
    Scientists at BIND Biosciences developed nanoparticles loaded with drugs that can effectively target tumors by staying in the bloodstream for more than a day. They hope the nanoparticles, which are coated with cancer-targeting proteins, can minimize side effects of chemotherapy. MIT Technology Review (11/4) LinkedInFacebookTwitterEmail this Story
  Company & Financial News 
  • Merck finalizes $41 billion merger with Schering-Plough
    Merck & Co. completed its $41 billion takeover of Schering-Plough, allowing the companies to begin operating as one entity today. The consolidation is expected to dramatically boost Merck's global expansion while bringing in a diverse pipeline of treatments, including those for cancer, women's health and infectious diseases. Google/Agence France-Presse (11/3) LinkedInFacebookTwitterEmail this Story
  • Lilly seeks investors to expand subsidiary's portfolio
    Eli Lilly and Co. plans to increase funds and put more drug candidates into its subsidiary Chorus, a company executive said. The drugmaker is looking for financial backers rather than pharmaceutical partners to maintain its control over Chorus' early- and late-stage drug development, said Gino Santini, Lilly's senior vice president of corporate strategy and business development. The Wall Street Journal/Dow Jones Newswires (11/3) LinkedInFacebookTwitterEmail this Story
  • FDA clears PerkinElmer's genetic screening processor
    The FDA has granted 510(k) clearance to PerkinElmer for its genetic screening processor designed to help public health laboratories screen newborns for genetic, hematologic or metabolic conditions. The GSP tool can enable laboratories to run multiple tests on very small blood samples. The Boston Globe (11/3) LinkedInFacebookTwitterEmail this Story
  Global Developments 
  Featured Content 
 

  Industrial & Environmental 
  • BP to ramp up biofuel production in coming years, exec says
    Philip New, CEO of BP Biofuels, said the company and its partner Verenium could make grass-derived ethanol for commercial consumption in the U.S. as early as next year. BP also plans to start commercial production of biobutanol by 2012 or 2013 at its proposed U.K. facility, which is expected to become operational in 2010, he added. Reuters (11/3) LinkedInFacebookTwitterEmail this Story
  News from BIO 
  • Looking for new strategies for managing your company's cash flow during this economic lull?
    Now is the time to check out BIO Business Solutions, BIO's cost-savings program. With 15 money-saving opportunities with leading providers in the biotech industry, saving your company money is made easier with BIO Business Solutions. Participation is free to members of BIO and 38 state/regional biotech associations. Get a complete list of the products and services available to you here. LinkedInFacebookTwitterEmail this Story
Learn more about BIO ->Conferences  |  Join BIO  |  Media  |  Issues  |  Industry

  SmartQuote 
If you smile when no one else is around, you really mean it."
--Andy Rooney,
American journalist and commentator


 
 
Subscriber Tools
     
Print friendly format | Web version | Search past news | Archive | Privacy policy

Advertise
Account Executive:  Chris Pope 202-737-5500 ext. 295
 
Read more at SmartBrief.com
A powerful Web site for SmartBrief readers including:
 
 
 Recent BIO SmartBrief Issues:   Lead Editor:  Ashley McMaster
     
Mailing Address:
SmartBrief, Inc.®, 1100 H ST NW, Suite 1000, Washington, DC 20005
 
 
© 1999-2009 SmartBrief, Inc.® Legal Information