The Michigan Center of Medical Research supports studies at a variety of sites throughout Michigan.
MICHMER’s site management services include:
Site feasibility and qualification according to protocol requirements
On-site training for the investigational team and the study staff
Patient recruitment services using internal call center
Archiving trial documentation and quality control
Centralized management and monitoring of sites, with IT support
Our monitoring activities involve feasibility and study site initiation, study development monitoring and study close-out at the clinical site. Our staff is trained to clarify protocol issues with the investigational team, handle protocol amendments, review the source documents related to clinical study data, report the advance events, and ensure patient safety and enrollment procedures.
MICHMER’s clinical monitoring services include:
Pre-study site evaluation and investigator assessments
Regulatory document preparation and collection
Budget and contract negotiation
Documentation maintenance and update
Site Initiation, interim and close-out site visits
Clinical study material accountability