Clinical Research in Québec, Canada
For 19 years, Diex Recherche has been a key player in clinical research in Québec, Canada, with six private clinics located at the heart of medical services.
Why choose Quebec (Canada) to conduct your clinical trial?
- Rapid approval from Health Canada
30 day processing times
- Strong Patient Compliance
High retention and stickiness rates
Universal access to the public health system
- Robust vaccination culture
Free vaccination program for many diseases
High-quality provincial vaccination registry
- Experienced clinical research sites
Network of sites with recognized expertise
- Diversity
Canada is one of the most diverse countries in the world
By 2036, around 30% of its population will be immigrants
Canada, a destination of choice for CROs/Pharmas
Therapeutic Areas
Getting the expertise, you need isn’t always easy
DIEX’s medical team will give you honest advice on your project from the beginning until the end.
Our team includes:
- Family Physicians
- Gynecologists
- Gastroenterologists
- Psychiatrists
- Medical Biochemists
- Rheumatologists
- Dermatologists
- Internal medicine Specialists
- Cardiologists
- Infectiologists
- Endocrinologists
- Pulmonologists
- Urologist
- Neuropsychologists
Access to Results
Speed & Transparency
DIEX uses secure digital systems (eSource, electronic records) for real-time tracking.
Optimized Recruitment
Database of 100,000 patients and collaborations with partner clinics.
Specialized Services
Endoscopies, biopsies, FibroScan®, sleep lab, psychedelic trials.
What DIEX can offer that others don’t, in our own private setting
- DIEX has over 100,000 patients in its databases in addition to all medical clinics near the DIEX sites
- Head Office (Leadership one point of contact)
- Almost 20 years of existence, with a proven track record
- All six sites are located in the heart of medical services
- All six sites are under the same SOPs and source documentation and are supported by the same leadership team
- Phase I to IV (outpatient) capacity
- Scalability in terms of resources to enable high-volume recruitment
- Multiple routes of drug administration expertise
- Virtual monitoring with eSource and Electronic site master file access
- Virtual Trial experience
- Notorious for our start-up and site readiness timelines
