Study Design and Protocol Development

IMD provides protocol development. More information about trial design is available at Trial Design under Consulting.

Study Management

IMD recruits and qualifies investigators, plan and executes all trial activities in collaboration with the sponsor.

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

IMD supplies CFR part 11 compliant data management either with paper CRFs or using a proprietary eCRF. 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. IMD provides full analysis and writing of clinical trial reports.

Publications

IMD provides publication services for the trials we analyze.