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Study Group: Emergency Medicine Physicians (US)(?)

Council Members in this Study Group: 1096

This study group may include physicians, care providers, and researchers specializing in internal medicine, cardiology, oncology, dermatology, emergency medicine, family medicine, neurology, obstetrics-gynecology, psychiatry, radiology, nursing, optometry, genetics, and mental health. It may also include experts knowledgeable on diagnostic labs, disease management, medical devices, long term care, surgery centers, health management, pharma, and biotechnology, among others.

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GLG NewsSMAnalyses by this Study Group's Experts(?)

Opinions and analyses expressed in GLG News are solely those of the author. See the Terms of Use for details.
Statistics can prove anything | 06-12-2008
Author: GLG Expert Contributor

Calling a 0.89% improvement "significant" just seems to me to show the weakness of this current trial.  Anyone can use statistics to prove just about anything.  Using verbal manipulation to puff up a study's result is unfair, unreliable and just plain sad.

This is going to be a huge fiasco | 06-12-2008
Analysis of: Researchers Fail to Reveal Full Drug Pay | www.nytimes.com
Author: GLG Expert Contributor

When the new administration come in, medicine and big pharma are both going to be hit hard.  Industry sponsored research is going to be examined with a fine tooth comb.  All we need is another scandal.  It's getting harder and harder to trust industry sponsored research, with news coming...

Thrombus aspiration with the Medtronic Export: the new standard PCI approach? | 05-30-2008
Author: GLG Expert Contributor

Percutaneous coronary interventions are standard therapy for both acute MI patients as well as unstable coronary syndromes, and are commonly utilized as preventive therapy in some patients. The practice of thrombectomy prior to stenting in these patients is simple and fairly risk-free, but...

Head to Head Comparisons will Help Patients but Hurt Profits | 05-27-2008
Author: GLG Expert Contributor

Direct comparisons between potential competing agents often do not exist Initial FDA approval is usually based on comparisons to placebo A new approval does necessarily mean that the new agent is better than existing ones, although this is implied by industry Industry bears all the costs of efficacy...

Time is of the essence | 02-21-2008
Author: GLG Expert Contributor

To be successful enrollment will have to be done in a mildly involuntary mannner. ie "You will be enrolled but can opt out by doing xyz." The ultimate test of such plans will be the willing acceptance by patients of disease management programs. Occasional inducements such as discounts...

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