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:

Investigators enrollment

Pre-study site evaluation and investigator assessments

Regulatory document preparation and collection

Budget and contract negotiation

Staff training

Documentation maintenance and update

Site Initiation, interim and close-out site visits

Clinical study material accountability