State-of-the-art Simulated Use Research Facilities
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.
State-of-the-art Simulated Use Research Facilities
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.
State-of-the-art Simulated Use Research Facilities
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.
Let's work together!
Contact us to discuss how we can advance your medical device development efforts together.
Let's work together!
Contact us to discuss how we can advance your medical device development efforts together.
Let's work together!
Contact us to discuss how we can advance your medical device development efforts together.
