info@irwcro.com | +46 8 791 66 40
19
JUL
2013

Experience

With more than 19 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
18
JUL
2013

Medical writing

Our medical writers work closely with Sponsors, Statisticians and Medical Advisers in order to develop study protocols, clinical investigation plans and study reports in accordance with current regulations and guidelines. The Medical Writers collaborate with the project team, and participate interactively throughout the study, from protocol to final study report. Services IRW offers medical writin