CLINICAL MONITORING

WHAT WE DO

PERI provides consistency and indication expertise in a progressive environment. We always look to monitor in the most efficient and effective manner while maintaining best in practice industry standards. PERI CRAs are nationally located minimizing travel time and cost to promote and support higher productivity and output. Unlike most CROs that overtask their staff, PERI CRAs average approximately three protocols at a given time, so they can focus on understanding the indication and protocol, maintaining site relationships, and monitoring precisely.

PERI DIFFERENTIATORS

Monitoring Strategy: PERI balances central data review, remote, on-site and targeted monitoring in order to ensure data is efficiently monitored in a cost-effective manner. PERI’s adaptive monitoring process supports the dynamic clinical monitoring environment. 

Site Relationships: CRAs cultivate and maintain strong relationships with PERI’s network of sites. CRA assignments are based both on location and experience at the site, supporting continuity of service.

Dedication: PERI CRAs work closely with the clinical trial operations team to effectively manage the clinical trial data. The collaborative environment supports high quality performance for all phases of clinical trials.