A well executed aggressive start helps set the pace for your study. Impact will mobilize resources quickly and efficiently to meet your timelines. Impact’s customer focus and resource flexibility assists your team in overcoming potential obstacles. We understand that an experienced team is critical in ensuring your trial runs smoothly. From experienced clinical trial monitors who know how to work with both sites and sponsors to accomplish data goals to project managers who can formulate clinical plans and develop comprehensive strategies, Impact has the experience and expertise to get the job done right.
Impact writers have extensive experience supporting clinical documents from IND submission through post-marketing commitments.
Impact offers comprehensive clinical trial monitoring and site management services from feasibility through site closeout to support clinical trials.
Impact project managers are highly skilled, experienced and integrate seamlessly with your team in order to deliver high quality, effective support.