Presa Clinical Research provides you with...

Site management: Includes support, documentation, and training
Data management: Includes collecting, managing, and reporting clinical data
Protocol compliance: Includes reviewing site records, monitoring reports, and ensuring compliance with regulatory standards
Site visits: Includes qualification, initiation, routine, and close-out visits
Training: Includes training on protocols, indications, and good clinical practice (GCP)
Auditing: Includes independent assessments of compliance with clinical trial protocols and regulatory requirements