With more than 20 years experience of conducting clinical trials and medical device development, 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 IV, including pediatrics, rare diseases and non-interventional studies and all classes of medical device investigations.
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.
IRW has offices in Denmark, Finland, Norway and Sweden, all with experienced and professional local staff. This gives you access to our network, e.g. for feasibilities. It also secures that local requirements for submissions to the Ethic Committees and Regulatory Authorities will be adhered to. Pan-Nordic presence is invaluable in reducing approval process timelines and it also facilitates the communication with all local parties involved in the project.
Several of our studies have been subject to audits and inspections, with favorable results in each case.