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Facilities and Services

For nearly 30 years, we have served as a trusted partner to academia, industry, government, and global health agencies, successfully advancing vaccine research through early discovery, controlled human infection models, Phase I–IV clinical trials, and real-world effectiveness studies.

Our Facilities & Services

Cutting Edge Facilities

CCfV boasts a range of specialized facilities, including on-site CL2 and CL3 laboratories, dedicated clinical spaces, and a state-of-the-art Challenge Unit. GMP BioLabs East, a small scale biomanufacturing facility due to come online in 2027, will increase our capacity by adding GMP production space, additional CL2 labs, and academic scale vaccine production.

Commitment to Quality and Innovation

CCfV’s end-to-end capabilities include preclinical studies, Controlled Human Infection Models (CHIMs), Phase I–III clinical trials, Phase IV post-market evaluations, disease surveillance, and socio-behavioral research addressing vaccine hesitancy, access, and uptake. This comprehensive portfolio is supported by in-house laboratory, data, and administrative infrastructure that enables high-quality research execution.

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Discover how CCfV can support your research.

At CCfV, we combine cutting-edge infrastructure with unparalleled expertise to deliver exceptional outcomes in vaccinology research. Join us in shaping the future of healthcare.

Contact
Sedric Pankras
Senior Manager, Business Development
sedric.pankras@dal.ca

User Access Policy

CCfV welcomes academic, industry, non-profit and government partners and collaborators at its facilities. Pending a request for access from any potential user, CCfV’s Operations Committee reviews the request for feasibility, scientific merit, financial viability, and risk to ensure that projects reflect the organization’s commitment to equity, diversity, and inclusivity. Priority access is provided to Canadian academic, government, and NGO users, followed by for-profit or industry users. Projects focused on research that may benefit underserved or special populations are also given a higher priority; recently, CCfV successfully collaborated on multiple projects with Indigenous communities (Nunavut, Nunatsiavut, Mi’kma’ki); Canadians of African descent, and international populations in developing countries (Bangladesh, Burkina Faso, Senegal).

For projects led or initiated by academic, publicly funded, or non-profit users, CCfV develops at-cost budgets with preferential pricing. CCfV budgets are based on a cost-plus margin for industry and for-profit groups. A full feasibility assessment is conducted once the Operations Committee determines that the requests meet CCfV’s standards and strategic goals. The user request then undergoes protocol/project review by a Principal Investigator; protocol, budget and deliverable review by the CAO and Associate Directors to assess feasibility and determine risks; and contract or agreement review in association with legal counsel to assess institutional and investigator risk and responsibilities.

Pricing is based on several factors and is developed through a three-tiered process. An initial high-level quote can be provided based on the estimated service requirements, with a more detailed budget to follow review of an executive summary of the proposed activities and/or projects. A final budget will then be developed based on the finalized protocol or statement of work, to be agreed upon by the Scientific Director, CCfV, Chief Financial Officer, CCfV, and potential collaborator(s).