Clinovative Research, Inc (CRI) has worked on several protocols with partners from other CROs and pharmaceutical companies.  In many of these cases, CRI is called on to augment ongoing services when monitoring frequency needs to be increased, there are issues with current monitoring practices, or there are problems with site compliance.

CRI is adept at reviewing current practices and providing fresh input to mobilize a stalled study or improve consistency among monitors.  We can provide project management assistance to help with timeline, budget, or staffing issues and can rally resources to maximize efficiency.  Our Clinical Research Associates have all provided oversight monitoring, onsite training, and co-monitoring for projects in various stages of completeness.  Our motto is to capitalize on the current best practices while bolstering areas of opportunity.  We do this through a partnership approach with you, the site, and/or other vendors to strengthen all team members involved in the project 

Regardless of your obstacle, CRI can give you the extra assistance you need to revitalize your clinical trial.