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About Us

IMARC Research, Inc. assists clinical researchers with obtaining the approval necessary to bring the latest medical devices, technology or pharmaceutical drugs to those who need them most.

We do this by providing cost-effective monitoring, auditing, training and consulting services to research sites and staff. Training is so vital to success in this field that we wanted to make it more accessible to everyone, from aspiring monitors to research sponsors and sales professionals.

That’s why we’re proud to launch IMARC University, a series of affordable online training and continuing education courses designed to prepare you and your team for clinical research compliance. These courses cover many aspects of the clinical research process, from FDA regulations and GCP standards to adverse event reporting and advanced monitoring topics. All courses can be taken at your own pace. We even offer customized training to meet the needs of your team.

Our staff developed these courses based on our robust curriculum for training our own clinical research monitors and auditors. Because our team frequently spends time at clinical research sites, we bring our extensive experiences and insights to each training course. IMARC University offers individual courses that allow you to pay per class, as well as packaged courses and role-based training courses.

Our courses are compatible with current versions of most major browsers, including Internet Explorer, Safari, Mozilla Firefox, and Google Chrome.


IMARC will ensure your team is up to speed for your clinical trial, from understanding adverse events reporting to knowing what FDA inspectors will look for when visiting your site. Regardless of where you are in your career, these courses will help you achieve the next level of proficiency.


Download our course catalog here for more details on our courses!


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