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.