Rare Disease

A dedicated cross-functional team of experts, made up of strategic leadership and tailored support for rare clinical trials

We turn patient voices into better data. We are focused on urgently accelerating the clinical development of new treatments in rare diseases, combining deep industry knowledge with personal experience to be your tailored research partner - building each study around individual patient needs with an agile team structure.

Clinical Development Delivery

Our rare disease experts provide the strategic vision and roadmap to facilitate full service clinical research delivery. There are clear advantages in small patient populations when using this type of offering coupled with our agile approach to both patient and customer needs.

Our service delivery approach enables us to provide global access to local resources in excess of 100 countries; operational hubs across Canada, US, Europe and India that are the backbone to driving project delivery; and expert insight from a highly experienced, focused leadership team, who can tailor the approach to project delivery on an individualised basis.

Combining our industry knowledge alongside personal experience within rare disease clinical trials makes us a more valuable research partner for Sponsors looking for a truly tailored service experience — we build studies around individual patients’ needs, with a nimble team that is never too far removed from the patient.

Patient Recruitment and Retention

Close relationships with patient advocacy groups, KOLs and patients
Established site networks for efficient startup timelines
Resources to support investigators and decrease trial burden
Deep understanding of inclusion/exclusion criteria to reduce screen fails
Strategic partnerships with grassroot and global patient organizations

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Resources

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Whitepaper

Patient Recruitment and Retention

What we do

Tech & AI

CRO Services

Resources

Rare Disease

Clinical Development Delivery

Patient Recruitment and Retention

Close relationships with patient advocacy groups, KOLs and patients

Established site networks for efficient startup timelines

Resources to support investigators and decrease trial burden

Deep understanding of inclusion/exclusion criteria to reduce screen fails

Strategic partnerships with grassroot and global patient organizations

Schedule a Meeting

Explore Helpful Resources

Challenges of conducting clinical trials in rare hematologic disorders

Challenges in Rare Ophthalmology Trials

Cellular and Gene Therapy

Cell Therapy for Multiple Myeloma

Rare Disease

Clinical Development Delivery

Patient Recruitment and Retention

Close relationships with patient advocacy groups, KOLs and patients

Established site networks for efficient startup timelines

Resources to support investigators and decrease trial burden

Deep understanding of inclusion/exclusion criteria to reduce screen fails

Strategic partnerships with grassroot and global patient organizations

Schedule a Meeting

Explore Helpful Resources

Challenges of conducting clinical trials in rare hematologic disorders

Challenges in Rare Ophthalmology Trials

Cellular and Gene Therapy

Cell Therapy for Multiple Myeloma