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The way FDA analyzes recalls and applies its list of root-cause possibilities needs a dose of transparency.
Reports that the online retailer wants to become a major hospital supplier is giving some in medtech reason to worry.
A doctor at Cedars-Sinai Medical Center explained how virtual reality technology is impacting patients suffering from chronic pain at MD&M West.
For successful device implementation, it's critical for medical device companies to provide support at all stages of the buying cycle.
Early compliance to the European Medical Device Regulation could give medical device manufacturers access to a potential $16.5 billion in revenues across the top 10 EU markets and Switzerland.
Medical tourism, an aging population, and a growing middle-income class are driving rapid growth in Thailand's medical device market.
This was the question one MD&M West speaker was asked to ponder as he addressed the convergence of consumer and medical technologies, and what that trend means for product design.
Your CAPA process should be entirely risk based, from the moment a request is made until you have verified the effectiveness of the actions taken.
New tools have given engineers have the ability to prototype rapidly, cheaply, and often, so how do you resist the urge to iterate endlessly?
An FDA initiative, now in its pilot phase, is helping the agency and medical device manufacturers see quality assurance in a new light.
An R&D professional with tricks up his sleeve showed MD&M West attendees how to apply the art of magical illusion to their next product development project.