Date: October 24 (1 day)
Price: 6900 SEK per participant
Place: Digitally
Course language: English
Diploma: Certificate is awarded after completion of the course
This course will cover (1) Regulatory medical writing which will visualize and create the documentation that regulatory agencies require in the approval process for drugs, devices and biologics. This includes clinical study protocols, clinical study reports, patient informed consent forms, investigator brochures and summary documents.
Educational medical writing (2) means writing documents about drugs, devices and biologics for general audiences, and for specific audiences such as health care professionals.