For Collaborators & Study Sponsors
We are not your typical clinical research site.
We offer so much more.
Customized support for your study – from idea to impact
Application & Design
Study Document Preparation (Protocol, ICF)
Participant Recruitment, Screening & Enrollment
Data Collection & Entry
(using HIPAA, PIPEDA & PIPA compliant research software & E-Consenting ability)
Subject Matter Expertise
Data Analysis Planning & Execution
Internal White Papers
From design to execution, we offer the support you need for your project.
Our highly qualified study team can test your idea or product at any phase.
We are a large, state-of-the-art clinical research centre equipped with the following tools and facilities:
What to Expect
We commit to providing top-quality support for your research studies.
Our team will walk you through all the steps of conducting clinical research.
Good Clinical Practice
Not only do we follow good clinical practice (GCP), we are certified to teach it.
We were brought on as a “rescue-site” at the 2-year mark during a pivotal, international clinical trial supporting FDA and Health Canada applications. We exceeded enrolment targets and completed the study within 9 months and were the first clinic in Western Canada to adopt the technology after its approval.
We were the first to test the use of a neuromodulation technology in a rare, off-label condition within the context of an N=1 case study; this ethics-approved study will be submitted for publication. We also met enrolment targets for the world’s largest normative database study in EEG-based neurotech.
We doubled our recruitment target after exceeding both enrolment and quality expectations for an industry-sponsored US Department of Defense funded post-approval clinical trial. Enrolment was competitive across four world-renown medical centres in the United States and Canada.