Integrated^®
Medical
Development

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Study Design and Protocol Development
IMDCRO provides protocol development under guidance from the consulting arm of IMD. More information about support of trial design is available at Trial Design.
Study Management
IMDCRO recruits and qualifies investigators, plan and executes all trial activities in collaboration with the sponsor. IMDCRO supplies IWRS for treatment allocation and test agent supply.
Medical and Site Monitoring
Medical Monitoring is done by industry experienced research physicians and site monitoring is provided through a regionally based force of monitors.
Data Management
IMDCRO supplies CFR part 11 compliant data management. IMD puts emphasis on CRF design, executing data management concurrent with clinical trial conduct, and close collaboration with the Clinical Research Associates to minimize the need for queries.
Mathematical and Statistical Analysis for Informative Reporting
Care is taken to understand data through secondary analyses as a basis for meaningful reporting. IMDCRO provides full analysis and writing of clinical trial reports.
Publications
IMDCRO provides publication services for the trials we analyze.