CDS Project Managers are ready to direct your entire product development program or provide select services according to your organization’s needs, ensuring meaningful outcomes at every stage of your product development.  

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CDS offers complete clinical trial management services in Canada and in the U.S., consisting of site selection, monitoring, quality assurance, project management, and post-market pharmacovigilance.  

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Backed by years of hands-on experience, the Regulatory Affairs team at CDS has insights to guide you in the best strategic direction at the outset of your product development plan.

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CDS designs regulatory strategies tailored to your product and its stage of development to summarize critical development issues and to track key milestones for your project.  

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Bring your pharmaceuticals to market faster with strategic plans designed by CDS. Partner with CDS to accelerate your goals and optimize your available resources. In finding the most efficient and most cost-effective route, CDS can take your products from pre-clinical trials to regulatory approval.

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In providing expert design in line with regulated quality assurance policies and procedures, CDS can build functional, reliable quality systems to anchor your organization’s operations. As a result, CDS clients see a reduction in errors, project time, in addition to cost and resource optimization.

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With extensive knowledge of regulations, CDS offers complete pharmacovigilance services in Canada and in the U.S. Whether you require safety rewporting during clinical trials or post-market approval, CDS safeguards your participants, partners, and study with perceptive safety intelligence.

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Whether you require writing for an integrated part of clinical development expertise, or a stand-alone service, increase the impact of your medical and scientific program with the help of our experienced team. 

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