Our approach to monitoring goes beyond following a checklist. Our team brings critical thinking and practical experience to your site to devise and implement the most effective strategies.
Our auditing programs provide an efficient, process-level assessment of Good Clinical Practice at research sites, sponsors, IRBs or vendors. We assess inspection readiness and prepare your team for success.
The Data Safety Monitoring Board and Clinical Events Committee provide objective oversight, adding credibility to your study. IMARC's established networks with physicians and specialists provide comprehensive safety monitoring so you can be confident in your results.
Our team brings exceptional leadership and measurable process improvements to any trial, based on nearly two decades of experience in the field. With our staff at the helm, your study will avoid common pitfalls, progress faster and more efficiently and ensure study compliance.
Let IMARC handle the paperwork, data entry and other site responsibilities so your research coordinators can focus on your study’s subjects. We offer comprehensive site support to enhance your team’s efficiency.
Cumbersome, absent or unfocused processes can overcomplicate your study or worse, set you up for noncompliance. Our consultants will evaluate your department's weaknesses and address your needs.
A well-trained staff is key to the success of your clinical study. That's why IMARC University offers comprehensive in-person and online training that can be customized to meet the needs of your team or individual staff members. Our training programs have been developed to ensure researchers understand the regulations as well as best practices and how to apply them using critical thinking skills.