Your Research. Our Expertise. Better Outcomes.

We leverage our strong local presence in Alberta, Canada, and deep connections within our communities to recruit diverse and engaged participants for every study.

Using a mix of digital marketing, patient advocacy, and grassroots efforts, we reach qualified participants efficiently.

Our commitment to inclusivity ensures access to participants from varied demographics, health profiles, and cultural backgrounds, resulting in comprehensive and reliable data.

With a track record of exceeding enrollment targets, we deliver timely recruitment solutions to keep studies on schedule.

Both of our locations feature on-site laboratory facilities offering on-site processing capabilities, including ambient and refrigerated centrifugation equipment. We offer specimen storage options such as -20 and -80 degree freezers.

Our team has extensive experience in collecting PK and PGx samples, ECG, manual and automated blood pressure devices, medical photography, ePROs, and more.

Both locations have diagnostic imaging facilities, located less than 4km from our site, and a nearby hospital ER adds even greater convenience and accessibility for our clients.

We offer refrigerated, frozen, and ambient IP storage with 24/7 data logging and automated warning and alarm notifications to ensure data integrity. Our IP is stored in swipe-card-only access rooms, ensuring the utmost security of the product.

Our use of the latest eSource and eISF technologies is CFR 21 Part 11 compliant. You can be confident in our procedures, as we have undergone an FDA inspection without receiving a Form 483 and a “Compliant” rating from a Health Canada Audit.

Our skilled investigators and coordinators bring expertise across multiple therapeutic areas, ensuring studies are conducted with precision and care.

From site activation to study closeout, our operational workflows are designed for efficiency, compliance, and minimal delays.

We adhere to all local, national, and international regulations, maintaining the highest ethical standards throughout the clinical trial process.

We prioritize the well-being of our participants, ensuring a positive experience that encourages study retention and long-term engagement.

Our use of advanced electronic data capture (EDC), electronic medical records (EMR), and real-time analytics enhances study accuracy and monitoring.

With secure, integrated systems, we ensure seamless data sharing and collaboration with Sponsors and CROs.

We embrace modern trial methodologies, including remote monitoring and decentralized trials, to expand accessibility and adaptability.

Our Sponsors and CROs receive up-to-date insights, empowering informed decisions throughout the study lifecycle.