To remove the barriers to RPM solutions, we need to empower application developers.
After a series of delays and false starts, EMA is now progressing its ISO IDMP agenda with firm intent. The first implementation guide is out now for consultation, to be followed by a second actionable version by next year. Life sciences companies targeting Europe will have a year to comply with all the measures—but this will be a lot of work.
The G4 gives doctors an additional range of clip sizes, along with enabling real-time procedure assessment.
The agency is encouraging the industry to develop sterilization approaches that either don’t rely on ethylene oxide or reduce emissions from this method.
Aging is not for the faint of heart.
The new method could help detect IBD, celiac disease, food allergies and other diseases much earlier.
Understanding the value of the VA and DoD device markets and how to best optimize access and revenue.
The agency is recommending that patients replace their affected pumps with models that can better protect against the risks.
This two-part virtual workshop will guide participants through the process of how to write effective documents.
The Class I recall involves complaints that the connector disconnects from the breathing unit.