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which reflects the FDA’s commitment to device innovation and protecting public health, is intended to help patients and health care providers receive more timely access to select medical devices.
The off-label use of drugs and devices by licensed physicians and the potential risk of harm experienced by consumers is an issue of much debate in the medical field. While the American and European ...
Drone814 plans to begin airlifting supplies across Greater Johnstown this summer through medical drone test trials – but that’s just the beginning, project partners said.
Drone814 partners plan to begin airlifting supplies across Greater Johnstown this summer through medical drone trials — in a ... operators to legally fly the devices outside their line of ...
"Our work will help ensure that these digital clinical trials are more diverse, equitable, and inclusive, and that new medical products that are safe, effective, and apply to all patients go to ...
Software as a medical device (SaMD ... Data is essential to the success of any clinical trial. When performing clinical trials of SaMD digital therapeutics, the device used must be capable of tracking ...
Med Device Makers need to re-apply for Compliance Certificates as CDSCO Introduces Automated Process
New Delhi: Medical device manufacturers and importers in India are now required to re-submit their applications for obtaining Market Standing Certificate (MSC) and Non-Conviction Certificate (NCC ...
Second Series A round co-led by family office of former Liberal leadership candidate Frank Baylis. Montréal-based medtech startup Puzzle Medical Devices has raised $43 million in a second Series A ...
The SecondWave MINI device employs “low intensity” focused ultrasound (LiFU) technology for spleen stimulation to treat acute and chronic inflammation disorders. It is currently under clinical trial ...
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