The Digital Medicine Society (DiMe) is partnering with PHTI, ZS, and other leading organizations to develop and launch core components of integrated evidence plans for digital health products to support faster regulatory approval and commercialization.
Veeva has launched a new tool to help MedTech developers identify and engage with healthcare experts and key opinion leaders.
The goal of the TAP Pilot is to reduce the time from concept to commercialization of medical devices by facilitating robust engagement early in the process with the FDA, industry and key stakeholders.
Participate in our new survey and have a chance to win complimentary access to the Computer Modeling & Simulation Virtual Conference on January 27–28, 2021.
Whatever the short- and longer-term fallout of COVID-19, organizations will need to come back fighting—with new tools at their disposal and ready to raise their game.
The hot issues are related to compliance, EU MDR and recalls.
Here are the most read articles of the year.
Bringing a product to market in the United States can be complicated, but it can be streamlined with a clear grasp of the process.