Clinical Trial Services

PCR Device Trials offers a full range of services, from project planning and protocol development through final report writing. We can provide solutions for some or all of your clinical trial needs. We also provide contract monitoring solutions.

Project Management: Our Project Managers share a passion and culture for working closely with our CRAs to stay on top of schedules, processes, reports, data integrity and timelines.

Translation Services: We offer translation services in 12 different languages..

Investigator Services: Site selection, qualification, investigator meetings, study agreements, initiation, regulatory document management, grant management and closeouts.

Monitoring: Our regionally - based CRAs with a world-wide reach, are experienced, knowledgeable, trained in GCP and constantly updated through continuing education.

Data Management: We provide state of the art solutions for data capture, validation and analysis including EDC, IVRS, fax form technology and traditional methods.

Outsourcing Services: We offer specialized laboratory and technical data expertise and provide external vendor screening, selection, budget negotiations, management, and specification document set up.

Biostatistical Analysis, Medical Writing and Regulatory Submissions by experienced, knowledgeable professionals.

Quality Auditing: We ensure best practices for study conduct, both internally and for our sponsors.