Medical Devices and Diagnostics

Medical Device and Diagnostics

Your world is unique – and quite different from pharma. In the U.S., decision-making has shifted from individual physicians to integrated networks--GPOs, IDNs and payers. These groups have heightened the focus on proving your solution’s value, demanding outcomes analyses and putting pressure on pricing.

How do leading innovators achieve MedTech success?

Leading companies trust IQVIA MedTech to enable clinical and commercial excellence using our fully integrated unparalleled data assets, consulting, and field solutions.

114

Countries provide global and local data

23.1M

Insights into healthcare professionals and 2.6M organizations

310+

Insights into HCP specialties and tendencies

1,000+

Insights into diagnostics and surgical procedures

1,400+

U.S. Market classifications

525K+

Unique SKUs covered in the U.S.

Making the Most of FDA's De Novo Classification Program

For companies looking to launch a novel, low-to-moderate risk medical device, new legislation permits the FDA to streamline the classification process under the appropriate level of regulation based on the novel device’s risk profile.
Which MedTech trends are important to monitor?
Staying informed on the MedTech industry’s top issues and evolving trends is vital for strategic planning. Our podcast series delves into these essential topics with industry experts.

MedTech capabilities

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