Our dedicated medical device and diagnostics team has the experience, knowledge and flexibility to meet the unique challenges faced by both emerging and established manufacturers throughout the product lifecycle.
Global expertise and resources to design, manage and monitor medical device and diagnostics clinical projects from first in human through large scale post marketing programmes.
Our regulatory and quality experts have extensive experience in working with medical devices, in-vitro diagnostics (IVDs), companion diagnostics and combination drug-device products and will help you achieve compliance in your chosen market(s) quickly and cost effectively.
As global regulatory landscapes shift and the convergence of the drug and device industries evolve, our dedicated team at ICON can assist with all phases of your clinical trial development and testing by supporting you in designing, implementing and managing clinical trials for your devices, diagnostics and combination devices to successfully bring your product to market, faster.
ICON has deep experience with the development and commercialisation of medical devices, medical device software, and in-vitro diagnostics covering all key therapeutic areas and indications.Explore
Resources and expertise to identify, generate, synthesize and communicate evidence of treatment value and safety, to help regulators, payers, providers and patients make informed health decisions.Explore
Integrated solutions based on the science of imaging biomarkers.Explore
ICON provides a full range of laboratory services that are dedicated exclusively to clinical development.Explore
Transform both organisational flexibility and operational productivityExplore
Develop the right business strategy to successfully navigate MDR/IVDR
Technologies that accelerate and improve clinical trials.
Design for the Patient Experience.
Late phase research, technology solutions and access to RWD are at the forefront of creating efficiencies in all stages of study design and implementation
The traditional healthcare delivery model is changing.
An adaptive design clinical trial can help to create a stronger value proposition for your medical device by reducing development costs and accelerating time-to-market.