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The Synapse Clinical Research Foundation (SCRF), a not-for-profit organization located in Delhi, India, has established a clinical trials registry to track research and development of medical treatments in the country.
An initial round of trade negotiations between the U.S. and South Korea in early June has “significant implications” for the device and diagnostics industry, AdvaMed said June 27.
A bill under consideration in the Massachusetts state legislature offers patients the option of giving their informed consent before being treated with reused, or "reprocessed," devices designed for single use only.
Lawmakers and government regulators need to consider the cost savings that devices and diagnostics offer to the U.S. healthcare system when making decisions that could affect patients’ access to new treatments, say industry leaders and at least one Senate lawmaker.
Phoenix Data Systems and Trio Clinical Research announced a new partnership at the Drug Information Association (DIA) annual conference in Philadelphia on June 20.
Electronic data capture (EDC) for clinical trials is proving to be a hassle for many research sites that have to keep on hand many separate systems for different sponsors, according to experts at a recent industry conference.
A recent policy decision by the Centers for Medicare & Medicaid Services (CMS) “simplifies physician billing for remote monitoring technologies” and will benefit thousands of cardiac patients across the U.S., devicemaker Medtronic said June 16.
Microsoft has accelerated its push into a variety of life sciences sectors, ranging from electronic track-and-trace technology to clinical trial management.
Change management and version control remain one of the toughest compliance challenges for FDA-regulated life science companies, a fact not lost on industry vendors and customers demanding more flexible tools, says a new study from International Data Corp. (IDC).