Where Are We Now With the Medical Devices Regulatory Framework?

Where Are We Now With the Medical Devices Regulatory Framework?

We all realise the importance of having a regulatory framework for medical devices. Medical products must be in border with certain directives so that private companies do not exploit the market with inferior and often unsafe products. Medical equipments are constantly improving along with fresh technological updates offering the industry superior products every year. This is a rapidly evolving field and the marketing of these devices is very profitable indeed. However, what about regulations? Where are we immediately with the medical devices regulatory framework?
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