Global Research Experts

Trust and confidence in local resources. With 15+ years of cooperation, our teams have a long history of collaboration to design, manage, and conduct global research. Since 2006, we have accumulated thousands of hours of scoping, bidding, executing, and delivering on global research programs.

Quality-certified systems. We have shared quality systems and processes across our companies. This supports a more seamless onboarding with your procurement team and offers your team confidence in our multi-country deliverables that data will be consistently collected and reported. We also have shared project tracking technology tools that enable us to see at a glance what is happening in each company. This helps us better resource projects, manage projects and budgets, and sync deliverables if necessary.

Regular communication, accountability, and responsiveness. Our management team is in constant communication to discuss local country nuances that can impact user research, like evolving COVID regulations, as well as best practices and industry trends. We also regularly jointly present at international conferences. This open line of communication also facilitates a comfort level to address any project challenges frankly and immediately.

International medical device research experts. Our global team of researchers are trained on international standards that define best practices in the application of human factors and usability engineering, including IEC 62366-1, as well as regional guidance where available, including FDA guidance, EU Medical Device Regulations (MDR), National Medical Products Administration (NMPA), and Medicines and Healthcare products Regulatory Agency (MHRA).