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Clinical Trials

Clinical Research Organization

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.

Stonington Global Testimonial

 

I am the owner and President of Stonington Global, a specialized law and consulting firm providing world-class personalized solutions to international clients. We have engaged dicentra on several different fronts, most recently for regulatory consulting and a clinical trial for a medical device. I would like to express that my experience in working with dicentra has been nothing short of ideal. They get back to me and my clients almost instantly. And they are very eager to please, valuing tremendously the potential continuum of every business relationship. What’s more, they completed our most recent study in 1/3 of the expected timeframe. My clients as well, which include NASDAQ listed players in the pharma, biotech, and medical device space, are also very pleased. I wholeheartedly recommend dicentra for any clinical trial work.

Nicholas D. Muzin

20

Years in Business

1,200

Clients Globally

6

Hospitals Within 1 Mile Of Our Clinic

6.4M

People Within 40 Miles Of Our Clinic

#1

The Priority and Care We Will
Devote to Your Project

dicentra's CRO Services:

Protocol Design

Protocol Review

Clinical Trial Monitoring

Multi-Centre Trial Management

Regulatory Submissions

Customized CRF / Source Document Design

GCP Compliance Auditing

Our clinical trial process from start to finish:

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.

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      *Please note: dicentra and all its subsidiaries only provide cannabis consulting services for business conducted in Canada, to the exclusion of all other countries.