A successful PI is one who knows the protocol well and is able to delegate specific functions to sub investigators and staff listed on FDA 1572 and on the Delegation of Authority document, while at the same time maintaining oversight and responsibility for all clinical trial activities. That means working with a team of trained and conscientious sub investigators and staff and ensuring that all patient eligibility criteria are met and that none of the exclusion criteria apply before enrolling a patient in a study. Smartpro Clinical will build out all aspects of your clinical research department ensuring that the clinical trials are followed, implemented and supported to provide the highest level of data integrity to the study sponsor. Research becomes an extension of your practice and we have the tools in place to make this happen in a most successful manner without interruption to your daily activities. We provide all support personnel and dedicate our time and effort for a successful outcome.
Our research is focused on improving patient outcomes and quality of life. We prioritize the needs and perspectives of patients in all aspects of our work. We work with the highest level of integrity.
We partner with leading pharmaceutical companies t to advance the field and bring new treatments and technologies to patients around the world.
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