Medical DevicesRegulatory Information ManagementRegulatory IntelligenceSoftwareTranslation Services

Software as a Medical Device Regulatory Intelligence

IQVIA

Booth: 428

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.

Other product: Cell & Gene Therapy Regulatory Intelligence

Other product: FDA Advisory Committee Regulatory Intelligence

Other product: Regulatory Intelligence

Other product: Regulatory Intelligence for Medical Device Clinical trials

Website FactsheetBrochure





Request Information





 
By requesting information, you agree to share the email you provided at the time of registration with the exhibitor for follow-up. Click on “Submit” to share your email or “Cancel” to cancel your information request.
 
 
Comments