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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

May 18, 2017

View Archived Issues

New CE mark rules make the FDA seem user-friendly for cardiovascular devices

PARIS – One week before regulations governing the CE mark for medical devices formally takes the force of law, makers of cardiovascular devices have already turned their backs on Europe and are headed to the U.S. for first-to-market approvals. Read More

Trump-proposed budget cut unites Congress in defense of the NIH

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3-D ortho company warned for incomplete cleaning validation

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Titan goes for single port approach in robotic surgical system market

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Study finds elderly patients easily adopt app-based, remote cardiac care monitors

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Appointments and advancements

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Financings

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Daily M&A

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Other news to note

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Product briefs

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Regulatory front

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MDD's Orthopedics Extra

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