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.
Ingredient suppliers and brand owners work with us to develop high-quality clinical research studies that help to identify how ingredients and products work, to document clinical safety and efficacy, and to provide support for unique claims to expand their product line globally.
Our team of medical and regulatory experts will help guide you through the process of clinical trial design and trial execution. We collaborate with you to build industry and consumer confidence in your brand through clinically demonstrated safety and efficacy. As your clinical trials partner, the mutual goal is to make a positive difference in the global health industry – by substantiating safety, quality, and/or efficacy.
Clinical Trials Across Our Team
Publications Across Our Team
Years in Business
Clients Globally
Hospitals Within 1 Mile Of Our Clinic
Participants Within Our Database
People Within 40 Miles Of Our Clinic
The Priority and Care We Will
Devote to Your Project
Protocol Design
Protocol Review
Clinical Trial Monitoring
Multi-Centre Trial Management
Regulatory Submissions
Customized CRF / Source Document Design
GCP Compliance Auditing
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.
Our team will work with you to identify the best possible approach to capture your most significant clinical outcomes through tactfully selected clinical analyses.
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.
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.
We will manage regulatory submissions to gain Health Canada and REB / IRB approval for your trial.
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.
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.
Strategic analysis of study results by an experienced team of biostatisticians to capture significant clinical endpoints.
Medical writing that captures your research and significant findings are prepared and for you to submit for publication.
Health claims made on natural health products must be supported by sound clinical research and are crucial to successful product development and marketing.
