We provide you with a simple process to get your clinical trial started. dicentra will help you design, manage, and execute your clinical trial to the highest level of regulatory and scientific quality.
Develop a Strategy
Our team will work with you to identify the best possible approach to capture your most significant clinical outcomes through tactfully selected clinical analyses.
Establish Budget and Timelines
Clinical trials can be costly and time-consuming but our team will work to ensure you stay within your clinical research budget and remain constantly aware of transparent timelines throughout the whole process.
Design Protocol
A well-designed protocol is critical to achieving your clinical research goals on time and on budget. Let us help you identify the best trial design, trial population and outcomes before designing the best possible protocol for your needs.
Obtain Approvals
We will manage regulatory submissions to gain Health Canada and REB / IRB approval for your trial.
Recruit Subjects
Recruitment is one of the most challenging aspects of a trial, let us take charge of finding quality research subjects to complete your trial safely and on time.
Conduct Study
Our clinical site in downtown Toronto will work to conduct your study with the highest regard for participant safety, data quality and ICH-GCP compliance.
Analyze Results
Strategic analysis of study results by an experienced team of biostatisticians to capture significant clinical endpoints.
Produce Reports
Medical writing that captures your research and significant findings are prepared and for you to submit for publication.
Substantiate Claims
Health claims made on natural health products must be supported by sound clinical research and are crucial to successful product development and marketing.