An intuitive interface and safety are the top priorities for today’s Medical device designers. Functionality and aesthetics both play a crucial role in making a device user-friendly. A John Hopkins study reveals medical errors account for 2,50,000 deaths and out...
What is SaMD? As per FDA, the term Software as Medical Device (SaMD) is Defined as “software intended to be used for one or more medical purposes that perform these purposes without being part of a hardware medical device.” Any software that helps...
The Canadian market has stringent regulations concerning Class I, II, Class III, Class IV Medical Devices. If you are someone looking to expand your product’s reach to Canadian markets, it’s important to understand the regulatory framework, requirements...
There has been a gradual shift in the Startup ecosystem in India. Three major influences controlling the economy dynamics, Government, Industrial, and Academia are collaborating to catalyze the process of innovation across the country. The reports by RBSA advisors...
What is Medical Device Contract Manufacturing? Medical Device Contract Manufacturing is a process where a MedTech company that owns the idea (sole proprietorship) outsources manufacturing to another Medical device manufacturing firm. The product is developed according...
Taking a me-too product to market is easy and comparatively less hectic as you just have to find a substantial equivalent (510k) to start selling. On the other hand, a new innovation led product requires much higher investment for clinical trials, documentation and...
