Conduct your medical device usability studies at ClariMed's purpose-built human factors research facilities across North America and Europe. Our network includes multiple specialized locations throughout the United States and our state-of-the-art flagship facility in Cambridge, UK, plus established partnerships with premium research venues worldwide.

Comprehensive Study Management Services

Our dedicated human factors study operations team handles every aspect of your usability study process:

• IRB/Ethics submission and approval management

• Targeted participant recruitment matching your exact user requirements

• Complete facility coordination and setup

• Equipment and research material procurement

• Full regulatory compliance oversight across all jurisdictions

Partner with ClariMed to ensure your human factors validation studies and formative evaluations are executed with precision, delivering the documentation you need for successful regulatory submissions.