Medhouse Academy

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Medical writing

Date: April  25 (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.

The lecturer for this course is Tanja Jensen. Communication, project management, and research has been the lion´s share of Tanja’s work for +10 year. This results in mainly two things. First, it results in driving global cross-functional teams at big pharma companies. With her teams, she ensures mainly regulatory documents related to clinical trials are built for decision-making and fit-for-purpose. Second, it results in creating and implementing educational material and workshops that boosts understanding and memory. Both things lead to reaching out with a message that makes an impact, while adhering to regulatory guidelines and fostering a fruitful team spirit.

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