SERVICES
Study Operations
With our expert study operations team, we efficiently manage all aspects of human factors and clinical studies.
Our comprehensive study operations services streamline the complex processes involved in conducting clinical studies and user research. From IRB management to participant recruitment, facility coordination, and procurement, we ensure that your studies are executed seamlessly and in compliance with regulations.
With a global network of usability experts and state-of-the-art facilities, ClariMed offers unmatched expertise in optimizing your medical product designs. Partner with us to leverage the power of human factors in your medical device development journey.
SERVICES
Study Operations
With our expert study operations team, we efficiently manage all aspects of human factors and clinical studies.
Our comprehensive study operations services streamline the complex processes involved in conducting clinical studies and user research. From IRB management to participant recruitment, facility coordination, and procurement, we ensure that your studies are executed seamlessly and in compliance with regulations.
With a global network of usability experts and state-of-the-art facilities, ClariMed offers unmatched expertise in optimizing your medical product designs. Partner with us to leverage the power of human factors in your medical device development journey.
SERVICES
Study Operations
With our expert study operations team, we efficiently manage all aspects of human factors and clinical studies.
Our comprehensive study operations services streamline the complex processes involved in conducting clinical studies and user research. From IRB management to participant recruitment, facility coordination, and procurement, we ensure that your studies are executed seamlessly and in compliance with regulations.
With a global network of usability experts and state-of-the-art facilities, ClariMed offers unmatched expertise in optimizing your medical product designs. Partner with us to leverage the power of human factors in your medical device development journey.
IRB Conduct
Navigate the Institutional Review Board (IRB) submission and approval process with our expert guidance and support.
Prepare and submit IRB applications and supporting documents
Communicate effectively with IRB staff and committee members
Address IRB questions and concerns promptly
Obtain and maintain IRB approval throughout the study
IRB Conduct
Navigate the Institutional Review Board (IRB) submission and approval process with our expert guidance and support.
Prepare and submit IRB applications and supporting documents
Communicate effectively with IRB staff and committee members
Address IRB questions and concerns promptly
Obtain and maintain IRB approval throughout the study
IRB Conduct
Navigate the Institutional Review Board (IRB) submission and approval process with our expert guidance and support.
Prepare and submit IRB applications and supporting documents
Communicate effectively with IRB staff and committee members
Address IRB questions and concerns promptly
Obtain and maintain IRB approval throughout the study
Recruitment
Identify, screen and enroll the right participants for your clinical studies and user research.
Develop targeted recruitment strategies and materials
Identify potential recruitment channels and partners
Screen potential participants for eligibility
Obtain informed consent from participants
Manage participant scheduling and communication
Recruitment
Identify, screen and enroll the right participants for your clinical studies and user research.
Develop targeted recruitment strategies and materials
Identify potential recruitment channels and partners
Screen potential participants for eligibility
Obtain informed consent from participants
Manage participant scheduling and communication
Recruitment
Identify, screen and enroll the right participants for your clinical studies and user research.
Develop targeted recruitment strategies and materials
Identify potential recruitment channels and partners
Screen potential participants for eligibility
Obtain informed consent from participants
Manage participant scheduling and communication
Facilities
Conduct your studies in appropriate and compliant settings with our facility management services.
Identify and select appropriate facilities for your studies
Ensure that facilities meet regulatory and protocol requirements
Manage facility scheduling and logistics
Coordinate with facility staff and stakeholders
Facilities
Conduct your studies in appropriate and compliant settings with our facility management services.
Identify and select appropriate facilities for your studies
Ensure that facilities meet regulatory and protocol requirements
Manage facility scheduling and logistics
Coordinate with facility staff and stakeholders
Facilities
Conduct your studies in appropriate and compliant settings with our facility management services.
Identify and select appropriate facilities for your studies
Ensure that facilities meet regulatory and protocol requirements
Manage facility scheduling and logistics
Coordinate with facility staff and stakeholders
Procurement
Access the necessary materials, equipment and services for your studies with our procurement expertise.
Identify and select qualified vendors and suppliers
Negotiate contracts and pricing to ensure cost-effectiveness
Manage vendor and supplier relationships
Ensure timely delivery of materials, equipment, and services
Procurement
Access the necessary materials, equipment and services for your studies with our procurement expertise.
Identify and select qualified vendors and suppliers
Negotiate contracts and pricing to ensure cost-effectiveness
Manage vendor and supplier relationships
Ensure timely delivery of materials, equipment, and services
Procurement
Access the necessary materials, equipment and services for your studies with our procurement expertise.
Identify and select qualified vendors and suppliers
Negotiate contracts and pricing to ensure cost-effectiveness
Manage vendor and supplier relationships
Ensure timely delivery of materials, equipment, and services
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.