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GLG News by Political Experts (outside Washington DC)

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Jeff StierFebruary 11, 2008
Consumer Product Safety Legislation Creates New Perils for Imports
Analysis of: Senate nears vote on product safety overhaul | www.reuters.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
This bill can significantly impact commerce.  Product liability and the ability to import products from developing countries may be acutely affected. Analysis includes not only who the bill hurts, but who it may help.
Jeff StierFebruary 8, 2008
WHO Declares Global War on Tobacco
Analysis of: World Health Organization Warns of Tobacco Use in Developing Countries | www.washingtonpost.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
The World Health Organization isn't going to let Altria's spinoff, Philip Morris International have a free ride in developing countries. With help from philanthropist New York Mayor Michael Bloomberg, the report highlights the scourge of global tobacco use, and efforts to get it under control.
Jeff StierJanuary 30, 2008
FDA… Today, Not Enough Regulation. Tomorrow, Too Much.
Analysis of: Growth of Genetic Tests Concerns Federal Panel | www.nytimes.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
Expect a window of opportunity in a wild west of genetic testing before abuse and a federal over-reaction.
Jeff StierJanuary 28, 2008
Activist Group Goes After Botox
Analysis of: Group Seeks New Warning About Botox | www.nytimes.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
A black box warning on Botox could harm Alergan (AGN).
Jeff StierJanuary 25, 2008
Good News For Drug-eluting Stent Makers
Analysis of: Drug-Coated Stents Safe, Study Concludes | www.washingtonpost.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
Two new studies add to the safety data of off-label use of drug-eluting stents.
Jeff StierJanuary 17, 2008
Lessons Learned from The Dr. Folkman "Controversies"
Analysis of: Famed Cancer Researcher Folkman Dies | ap.google.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
These lessons are valuable for considering new cancer research findings.     Just ask Genentech. Symbol: DNA
Jeff StierJanuary 15, 2008
As Long As There is a Cure, Does it Matter Whether There Is a (Real) Ailment?
Analysis of: Drug Approved. Is Disease Real? | www.nytimes.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
Pfizer(NYS:PFE)( :EQPFIZER), Eli Lilly and Forest Labs(NYS:FRX) are all hoping that it doesn't make a difference.
Jeff StierDecember 11, 2007
The Importance of the FDA's Stance on Merck's (and now GSK's) OTC Mevacor
Analysis of: FDA weighs over-counter cholesterol drug | news.yahoo.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
How will the FDA rule? What are the potential public health benefits? Are there risks of OTC statins?  Watching closely, will be Glaxo Smithkline (GSK), which will market OTC Mevacor. Approval could impact sales of Pfizer's Lipitor and other statins made by pharma's including AstraZeneca, Novartis...
Jeff StierDecember 5, 2007
Entire Tobacco Industry Must Take Notice At Three Judge Panel Ruling In MInnesota
Analysis of: Minnesota Court Reinstates Reynolds "Lights" Case | www.reuters.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
This should keep defense lawyers busy not only for defendant, R.J. Reynolds Tobacco Co., but Altria, (Philip Morris) and Brown & Williamson - as it opens the door to similar cases against them, pending in Minnesota. The case will be watched, and may even have (limited) impact, on similar cases in...
Jeff StierDecember 4, 2007
Report Slamming FDA May Be Just What The Doctore Ordered for FDA
Analysis of: FDA science dearth puts public health at risk | news.yahoo.com
Author: Jeff Stier, Associate Director, American Council on Science and Health
The report, while critical of FDA, is more of a slap at Congress than the agency. It may remind Congress that consumers as well as the biotech and pharma industries rely on a healthy FDA. Moreover, it should serve to remind Congress to exercise caution before giving the agency increased regulator responsibility-...

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