Target group
The workshop is aimed at those who write or review regulatory documents or are involved in documentation issues, such as service commissioners, statisticians or medical experts.
Learning objectives
After the day, you as a participant:
- Be aware of key regulations and guidelines that are relevant – how to find them, basic knowledge of how to use them and why it is good to use them.
- Feeling empowered in your role as a Medical Writer – having basic tools for planning and completing an assignment, what documents are required and knowledge of the interaction between different roles in your team.
- Know how to interact with the Medical Writer – for those working in other roles.
From the program
The day will focus on the ‘why’, ‘what’ and ‘how’ of Medical Writing, covering both pharmaceutical and medical device documents with a focus on study reports.
- What is the purpose of the most common regulatory documents? Why should you follow the guidelines?
- Which documents does a Medical Writer write – and how are they linked to each other?
- How should you write? What makes a good document? Do´s and Dont´s?
- How do you plan your writing? How to cooperate in a structured way between the roles?
For an interactive day, speakers will intersperse theory with questions, discussions and examples and experiences from their work.
The lectures will be held in Swedish.
Click here for more information and registration.
