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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 pediatri

Meeting your post-marketing pharmacovigilance, clinical study safety, or device vigilance obligations is a key requirement for your business. Does your company have the resources and know-how needed to continuously monitor the safety profile of your company’s products? Don’t worry, we can help you. Our pharmacovigilance team consists of highly dedicated, professional and experienced members from b