IRW Consulting AB, a Clinical Research Organization (CRO) was founded in 1999. We are currently represented in Sweden, Norway, Denmark and Finland.

We offer professional Clinical Trial Management for pharmaceutical, biotechnology and medical device companies with a wide range of clinical trial services.

IRW Consulting AB has a dedicated and professional team with a wide range of competencies and experiences from academic and clinical research, as well as experience from working with global pharmaceutical companies, biotech companies and various regulatory authorities in the Nordic region.

At IRW Consulting AB, we conduct our work according to ICH-GCP guidelines, The Helsinki Declaration and all applicable local regulations. Being a local CRO in the Nordic region, we can provide you with our knowledge on local networks including investigators both at the private sector and state-run hospitals.

IRW Consulting AB is highly aware that the pharmaceutical industry is keen on cutting timelines and being cost effective in bringing an investigational product right up to registration. As a result, we are committed to working along these principles for our clients.

Our team can either work independently or part of your project team, pending on your request.