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Research institutions might consider providing prospective monitoring when enhancing a research compliance program.
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Clinical trial sites and institutions that want to reduce errors and undesirable audit findings need to invest more resources in educating research staff, an expert asserts.
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Medical residents often lack the knowledge and skills they need to interpret medical research studies, which can jeopardize their ability to integrate new findings into their clinical practice, a recent study says.
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Over the past five years significant advances have marched out of the laboratories and clinical trial factories of the cardiovascular disease sector.
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On one level at least, Europe is only an idea. It has a flag and an anthem, but no constitution nor a mandate to regulate health policies and practices.
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Direct Flow Medical (Santa Rosa, California), a company developing a minimally invasive implant to treat patients with heart valve disease, reported completing its Series B financing and initiating clinical trials in Europe.
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In another move designed to deal with big debt and stagnating device sales, Boston Scientific (Natick, Massachusetts) reported its long-anticipated restructuring.
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ImaRx Therapeutics and Royal Philips Electronics reported a new research alliance focused on using Philips' ultrasound technology as part of ImaRx's SonoLysis program to develop a new treatment for acute ischemic stroke.
