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The human element of IoE changing the way breast cancer is detected #medicaldevice

The human element of IoE changing the way breast cancer is detected #medicaldevice

Are These Medical Devices Safe? (da Vinci Surgical System) | MDDI Medical Device and Diagnostic Industry News Products and Suppliers

Are These Medical Devices Safe? (da Vinci Surgical System) | MDDI Medical Device and Diagnostic Industry News Products and Suppliers

SI-BONE, led by CEO Jeffrey Dunn, raised $21 million in growth capital and brought on new CFO Laura Francis.

SI-BONE, led by CEO Jeffrey Dunn, raised $21 million in growth capital and brought on new CFO Laura Francis.

J&J lags in spine, trauma, diabetes and vision care but strong in electrophysiology, biosurgery - FierceMedicalDevices

J&J lags in spine, trauma, diabetes and vision care but strong in electrophysiology, biosurgery - FierceMedicalDevices

MedTech Workshop & Networking Event #2 - Entering the Market - 8th September 2015 - MedTech Learning

MedTech Workshop & Networking Event #2 - Entering the Market - 8th September 2015 - MedTech Learning

Use Systems Thinking When Developing #MedicalDevices

Use Systems Thinking When Developing #MedicalDevices

Innovation Has To Go Beyond R&D #medicaldevice

Innovation Has To Go Beyond R&D #medicaldevice

'The Food and Drug Administration declared the tiny vials used by Theranos Inc. to collect finger-pricked blood from patients an “uncleared medical device” that the laboratory company was shipping across state lines.  Inspection reports posted on the agency’s website Tuesday also showed that the FDA found deficiencies in Theranos’s processes for handling customer complaints, monitoring quality and vetting suppliers.'

FDA Inspectors Call Theranos Blood Vial ‘Uncleared Medical Device’

'The Food and Drug Administration declared the tiny vials used by Theranos Inc. to collect finger-pricked blood from patients an “uncleared medical device” that the laboratory company was shipping across state lines. Inspection reports posted on the agency’s website Tuesday also showed that the FDA found deficiencies in Theranos’s processes for handling customer complaints, monitoring quality and vetting suppliers.'

FDA rips Europe's system for medical device reviews

FDA rips Europe's system for medical device reviews

How Medical Device Makers Can Encourage Patient Engagement #medicaldevices

How Medical Device Makers Can Encourage Patient Engagement #medicaldevices

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