Conducting clinical trials is inherently complex, and engaging with sites is becoming even more competitive given limited capacity and increasingly overburdened site staff. In this environment, local knowledge and global […]
Our Clinical Site Managers will support your trial starting from the Services onset, through to Start Up, Clinical and Post Clinical Activities, and Project close out: Key contact with the […]
Our unique study delivery model to support Sponsors of Clinical trials: Provision of own independent teams of coordinators and nurses, Support with patient recruitment & engagement, Development of patient retention […]
With clinical trial nurses and physicians covering CEE, IRN can work with sponsors, CROs, and study sites to provide extensive services at patient’s home, including: Sample collection, Intravenous infusions, Injections, […]
Full strategic and operational support from our Regulatory Affairs team includes: Communication with the ECs and RAs on a regular basis Prepare and review regulatory applications Maintenance of regulatory intelligence […]
With our patient-centric approach of work we help you to achieve faster trial timelines, accelerate recruitment and keep patients engaged throughout the whole study. Our trained and experienced Clinical Site […]
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