info@irwcro.com | +46 8 791 66 40
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Do you need resources and
know-how to monitor the
safety profile of your products?

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Do you need a study protocol or
a report to be written by an
experienced medical writer?
Do you need information on
how patients perceive the
pharmacological treatment with
your product?

IRW is a Nordic full-service Clinical Research Organisation (CRO ) with local offices and staff in Sweden, Denmark, Norway and Finland and with more than 15 years of experience of Clinical Research Outsourcing in Scandinavia.

We offer cost efficient services in Clinical Operations, Project Management, Regulatory, Clinical Data Management, Biostatistics, Pharmacovigilance and Medical Writing for the whole range of customers from virtual Biotech and Medtech companies to Big Pharma and other CROs. We today have ongoing assignments in all development phases I-IV, medical device investigations, non-interventional trials and registry trials as well as projects where we use IRW’s own smartphone, tablet or web based electronic patient diaries for collection of electronic Patient Reported Outcomes (ePRO). We can manage your project from start to finish or function as a fully integrated part of your own project team.

IRW’s dynamic approach to the changing clinical trials environment in combination with our long experience and unique knowledge of the Nordic market with hand-picked staff for every assignment makes us uniquely positioned as the preferred Nordic CRO for our customers, whether it comes to providing in-sourced expertise or the conduct of highly complex projects.

We help you reach your goals, efficiently!

Services

We are expanding

We are now looking for new colleagues in all Nordic countries.
Read more about job opportunities under career page.
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