About Us
DAR Clinical Research is an innovative and unique provider of high-quality solutions for clinical trial facilities. We work together with research organizations and pharmaceutical companies to make clinical trials available to patients in Canada. The companies we work with are some of the largest and most respected organizations in the industry and we are proud to be able to provide our volunteers with access to their trial opportunities​.
We operate by an experienced team of officers and coordinators. We value the importance of our study volunteers in making clinical research possible. We are committed to providing eligible volunteers access to ethically approved research, and maintain the safety and integrity of the research environment to the highest standards.
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Our team strives to developing new business in the healthcare arena, taking advantage of the strengths of business alliance with medical institutions.
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Our Mission
To create value by accelerating the access to therapies that improve patients’ lives.
Our Vision
To advance innovation and provide solutions that will empower those that in the medical arena to achieve greater health and well-being.
Services:
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Site Management Organization Services include but are not limited to:
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Study Management
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IRB Management
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Site contract, budget expense management
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Enrolling and retaining participants, managing visits
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Patient safety management Safety and Adverse Events (AEs) Management
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Ensuring Protocol Adherence
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Ensuring Data Security
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Quality control
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Logistics management
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Archiving Essential Documents
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Archiving trial data
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Data Collection
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eCRF completion
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Investigator Site File Management
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We keep our processes and your projects under control through the implementation and oversight of our in-house, updated, precise Standard Operating Procedures (SOPs) or the Client’s SOPs.
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Site Management Models at DAR:
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Here at DAR we have two models of site management. In our Full Integration Service, we employ and train our coordinators and manage the accounting for these sites. We take on clinical trials and provide the necessary oversight outside of the principal investigator responsibilities.
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The other model is our Scope of Service model. Research site function semi-independently from DAR for day-to-day management, staff their own coordinators, however, we provide and manage our own quality programs. Site have the option to select what stage and scope of the clinical trial we can manage, Our main job, will always to ensure we are integrating or embedding research protocols into the ongoing function of the site.
