Software as a Medical Device Regulatory Intelligence
The number of new Software as a Medical Device products starting on their path to market are rising as fast as regulations are being developed. To prevent your company’s innovations being rejected for not meeting the changing requirements, your regulatory teams need to make sure that they can keep up-to-date. This means tracking new and evolving requirements, and their impact on new and existing products, as soon as they are released. Developed and maintained by IQVIA local experts and in-house medical device experts, IQVIA Regulatory Intelligence is a database that collects all the latest regulations as they are released across the EU, U.S., Japan, South Korea and China. By offering direct access to information on emerging regulations in key medical device markets, it helps you manage all new updates in order to accelerate your product forward.