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Do you require clinically meaningful patient-centered evidence to support regulatory submissions and health technology assessments?

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A New Era in Outcomes Measurement

With the recent push by regulatory bodies to include patient reported outcomes in all stages of clinical development, the patient voice is now a key element of any research protocol.

With 25+ years of experience, our approach provides the patient-centered outcomes research evidence needed for regulatory submissions and health technology assessments.

Patient-focused Research services, including:

Pre-trial Preparation:

Protocols and Statistical Analysis Plans

IRB Submissions

Qualitative Patient & Caregiver Interviews

Instrument Development

Goal Attainment Scaling Sponsor Workshops, Advisory Boards, Investigator Meetings

Bespoke Virtual Training Programs, Webinars, and Materials

Ongoing Studies:

Goal Attainment Scaling Support

Baseline, Patient Journey and End-of-Study Surveys

PCOR-Focused Electronic Data Capture

Data Management, Reporting, and Analytics

Medical Writing and Dissemination

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Local with a global impact

Based in Nova Scotia, our culture reflects an East Coast Canadian ethos rooted in hard work and collegiality.

With over a decade of experience partnering with multinational sponsors on cutting-edge patient-centric research, the impact of our work is global.

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