by Syrma Johari | Feb 12, 2022 | Blog
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...
by Syrma Johari | Feb 11, 2022 | Blog
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...
by Syrma Johari | Feb 4, 2022 | Blog
Labor pain is one of the most severe kinds of pain a women experiences in their lifetime. There have been many instances, where doctors have tried figuring out solutions to lower the pain without compromising the health of the mother and fetus. But, to everyone’s...
by Syrma Johari | Jan 31, 2022 | Blog
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...
by Syrma Johari | Jan 28, 2022 | Blog
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...
by Syrma Johari | Jan 13, 2022 | Blog
Getting your Class II Medical Device in US Market requires several steps of 510k clearance. Before you begin the submission it’s necessary to understand, what is exactly 510k? Medical Device Manufacturers and Developers must be ready with required documents to ensure...
