HSA
The new article describes in detail the approach to be followed when applying for registration and marketing approval for Class A and B medical devices.
HSA
The article outlines the key points associated with registering healthcare products under the existing legal framework.
Medical Devices
In today’s rapidly evolving regulatory landscape, medical device companies face increasingly complex challenges in managing compliance and bringing their products to market efficiently. As a regulatory professional, you’re likely all too familiar with the time-consuming and intricate process of preparing regulatory submissions. The use of AI streamlines this process to reduce errors, improve compliance and get your product to market faster.
FDA
The new article describes in detail the enforcement policy introduced by the authority and also highlights the key points to be considered in order to comply with it.
FDA
The article provides an overview of the regulatory requirements related to safety in the magnetic resonance environment and highlights the key points to be taken into consideration by medical device manufacturers and other parties involved.
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