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

Medical writing

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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 writing as part of a full-service program or as a stand-alone service. Our medical writing team supports preparation of the following:

  • Protocol Design for Phase I-IV clinical studies and Post Marketing Observational Studies
  • Informed consent form design
  • Case Report Form Design
  • Study specific questionnaire design
  • Written and tabular summaries
  • Medical and scientific literature reviews
  • Literature Search
  • Periodic Safety Update reports (PSURs) and other pharmacovigilance documents
  • Expert reports and executive summaries
  • Data Safety Monitoring Board (DSMB) manuals
  • Interim/Final study report preparation
  • Clinical study reports

Contact us:

Sweden
IRW Consulting AB
Svärdvägen 5, NB
Box 703
182 17 Danderyd
Ph: +46 735 196 042

IRW Consulting AB
Jonsereds Fabriker
Kanalstråket 1
433 76 Jonsered
Ph: +46 735 196 041

Finland
IRW Consulting AB Finland
Rajatorpantie 41C
FI-016 40 Vantaa
Ph: +46 735 196 042

Denmark
IRW Consulting ApS
IH-108, Center Boulevard 5
DK-2300 København S
Ph: +45 45 79 01 02


Norway
IRW Consulting NUF
Henrik Ibsens Gate 90
NO-0255 Oslo
Ph: +46 735 19 60 42

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Keywords
Clinical research, Clinical trials, Clinical research in Scandinavia, Clinical trials in Nordics, Klinisk prövning, CRO, Sweden, Norway Denmark, Finland, Data management, Pharmacovigilance, Clinical monitoring, Non- interventional studies, Medical writing, Clinical trial management, Outsourcing, Consultancy, Risk based study management, Biostatistics