IMARC, a clinical research organization, is introducing new services designed to better assist research professionals as they secure regulatory approval.
IMARC has been a trusted source of independent monitoring, auditing, training and consulting for nearly two decades.
The expanded offerings are a response to the growing needs of clinical research sites who often face high staff turnover or a lack of internal expertise.
“Though our team is capable of stepping in at any point in a clinical research trial, study sponsors see the best value when we are involved from start to finish,” said IMARC CEO Sandra Maddock. “We are able to offer comprehensive planning, consulting and oversight from all angles, ensuring the data is flawless and the study integrity is beyond reproach.”
IMARC’s new services include:
IMARC offers a single point of contact to coordinate with vendors and staff, providing measurable process improvements and enhancing efficiency. Our project management team ensures study compliance and helps clinical research teams bring their device to market faster.
IMARC University, our newly expanded training division, offers comprehensive in-person and online training, ensuring teams and individuals understand the regulations and how to apply them using critical thinking. Clinical researchers can advance their expertise and accelerate their career with convenient, affordable training through our online portal.
IMARC has established an extensive network of physicians and specialists to offer comprehensive safety monitoring from the Data Safety Monitoring Boards and Clinical Events Committees. IMARC will manage all administration of safety monitoring, from arranging and documenting meetings to providing Sunshine Act financial reporting.
IMARC will handle the paperwork, data collection and data entry and other site responsibilities so your sites can prioritize their time toward recruitment and retention.