Clinical Trials / Clinical Trial Research

We work with major brands and pharma companies to conduct top-grade clinical research studies.

These studies help us and you understand how biotech and pharma products work and how safe and effective they are. Such studies help brands make unique claims that can help expand their markets across the globe. 

Our Clinical Trials Process:

Device a strategy

We will work with you to vet the right clinical analyses and the best possible strategy to achieve your clinical outcomes. 

Set budgets & timelines

We manage your budget and keep you constantly aware of your progress through transparent timelines, and save you a ton of money by ensuring you stay within budget. 

Create a protocol

Your protocol design is vital to reaching your research goals on time and on budget. We help identify the best trial design, population and outcomes before devising the protocol most suited to your needs. 

Get regulatory approval

We will manage all regulatory submissions including Health Canada and REB/IRB approvals for your trial. 

Sign up subjects

Subject recruitment can make or break a clinical study, and we will find high quality research subjects appropriate to your needs and ensure you complete your trial safely

Execute study

Our site in Toronto will conduct your study with the utmost regard for subject safety, data consistency and regulatory compliance. 

Crunch the results

Our expert biostatistics team will capture the most significant clinical data points by strategic analyses of the test results. 

Create & manage reports

Our research helps substantiate unique claims made by pharma vendors and natural health product manufacturers. Unique claims substantiated by strong clinical data helps market your products across the globe and develop consumer trust. 

Support claims

Our expert medical writing captures your most significant results so you are ready to submit for publication.