Our Clinical Research Associates (CRAs) are an extension of our Sponsors. They are experienced at working effectively with sites to ensure patient recruitment and study execution goals are met.
We offer our Sponsors flexible approaches to monitoring, from full-service monitoring to centralized and risk-based monitoring, to achieve your goals and needs. With the ability to assign office-based or regional CRAs to your project, we take an approach that is the right fit for your clinical program focusing on data quality improvement and accelerated database lock.
The study’s integrity is of utmost importance to Nutrasource. Our CRAs ensure the highest quality data through the duration of the clinical project from site qualification through close-out, with specific attention paid to patient eligibility, protocol adherence and implementation, adverse event management and reporting, regulatory document maintenance and data collection, entry and accuracy.
Looking for more information on clinical monitoring? Contact a member of our team today or email us directly at firstname.lastname@example.org. You may also request a customized quote and we will contact you with details within two business days.