Clinical Research Expertise
ethica CRO offers specialized services to manage the unique and complex requirements of your dermatological studies. We provide insight and guidance to ensure optimal research participant experience and viable clinical outcomes.
ethica CRO provides a full range of tailored clinical research services for medical device research programs. From study start-up to closeout, achieve your unique study goals while mitigating risks and reducing study-related costs.
ethica’s vast network of medical experts, trained investigators, high performing sites and CROs across the globe is at your disposal to ensure effective conduct of your neurology clinical trials.
ethica CRO is your partner of choice for managing the many complexities of respiratory disease research. Our experience in this therapeutic domain includes asthma, cystic fibrosis, and chronic obstructive pulmonary disease.
Investigator Initiated Trials (ITT)
Don’t take any unnecessary risks with your Investigator Initiated Trials (ITTs). Leverage ethica’s experience and study management, data management, and biostatistical services, specifically geared to the needs of ITTs.
ethica CRO can introduce your therapeutic product to the North American and European markets. Discover myriad reasons that make Canada a wise choice for your clinical research project.
Get in touch
Have any questions about our clinical research expertise or want to submit a request for proposal from our CRO? Get in touch via our contact page we will get back to you as quickly as possible.