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IRW offers phase I-IV trial management, as well as all classes of medical device investigations, from single-center to multi-national projects. With more than 19 years experience of working with majority of indications and products, our competent, dedicated and flexible study teams are ready and able to deliver. We manage projects from start to finish, but are also happy to work as an integrated p

Efficient data management speeds the clinical trial process and ensures excellent data collection accuracy and consistency. We can meet all of your clinical data management needs. Our tools are extensively customized to meet your specific needs –both for paper-based and Electronic Data Capture (EDC)  trials. Our systems, SOPs and staff will provide you with cost-effective, secure, regulatory-compl

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. W

Please fill in the form below or contact us via phone or email. For general queries, call +46 8 791 66 40 or send an email at info@irwcro.com If you are a job applicant, please use the application form under the career section. Social Network