IRW is a Nordic Contract Research Organization (CRO) with more than 20 years of experience in conducting clinical trials, Non-Interventional Studies (NIS) and medical device studies. IRW has built an extensive network throughout all Nordic countries, as well as the rest of Europe and the US. Depending on the customer’s requirements, our staff is either outsourced or works with in-house projects. We cover all the stages of clinical development, from phase I to phase IV, including pediatric and non-interventional studies and all classes of medical device investigations.
With regional offices in Denmark, Finland, Norway and Sweden, IRW has experienced locally-based staff providing an optimum combination of local knowledge and expertise to assist you conduct your clinical trial as per country specific guidelines. Local presence not just ensures adherence to local requirements for submissions to the Ethic Committees and Regulatory Authorities but also the knowledge of local language facilitates the communication with all local parties involved in the project thereby avoiding possible misunderstandings and reducing approval process timelines.
Working with the full range of companies, from small start-ups to multi-national pharmaceutical corporations, we have learned how to tailor our services to the specific needs of our customers. Our involvement in clinical trials covers both Europe and the US, always following the appropriate regulations wherever we work, either according to external party’s SOPs or our own.
Several of our studies have been subject to audits and inspections, with favorable results in each case.