Take advantage of the fastest-growing clinical trials region to
accelerate your global clinical research.
Canada is a highly developed nation with one of the largest economies in the world. It performs strongly in international comparisons of quality of life, health, education, and other measures.
Canada is home to some of the world’s best medical researchers and health professionals and enjoys world-class research infrastructure equal to the US. Clinical trial capability is also of an international standard and the country is well suited to conduct complex trials that are generally focused on indications aligned with the standard of care in developed nations.
With streamlined regulatory requirements and the supportive R&D Government refund of up to 30.6% on clinical research spend, Canada has become a preferred destination for all phases of clinical trials.
Greenline Clinical Research has built strong expertise over the years in providing CRO services to biotechnology companies in Canada.
In Canada, biotechnology companies enjoy start-up timelines of around 6 to 8 weeks, from Ethics Committee (EC) submission to Health Canada approval.
Greenline Clinical Research’s Medical and Regulatory Consulting team offers full range of pre-clinical, regulatory affairs support, medical and pharmacovigilance consulting services.
Greenline Clinical Research relies on years of experience, in-country knowledge and real-life big data to identify and propose the best-performing sites for your study.
Canada is a preferred destination for early phase trials because of simple and fast regulatory stream and lucrative R&D cash refund scheme.
Greenline Clinical Research’s streamlined and integrated clinical trial services are delivered by a dedicated team of professionals with deep industry and therapeutic area expertise across all phases of clinical development.
Delivering accurate, high-quality and timely biostatistics in clinical trials services, including statistical planning, analysis and reporting.
How virtual clinical trials can offer patient retention and cost benefits compared to traditional trials.
Accelerating patient recruitment and drug development with real world data (RWD)
Our bioanalytical services assist our customers in every stage of their molecule development.
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