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Clinical Study Report Writing
Lund, Sweden

Clinical Study Report Writing

February, 04, 2010, Lund, Sweden

Description
The course includes a comprehensive survey of ICH E3 with tips on how to avoid the most common problems, how to simplify the writing process and how to structure quality control and review. The course will also briefly discuss when a complete clinical study report is not necessary and what to include in a report written under such circumstances.

• ICH E3
• Data presentation
• Quality control & review
• Preparation of appendices
• “Abbreviated clinical study reports”

Target group
The course is designed for anybody who is planning to or already has started to write clinical study reports. The course will also benefit anybody involved in review and quality control of clinical study reports and other medical documents. The course will be of most value to those who already have some experience in clinical development.


The course will be provided in English.

The number of participants is limited to 10.
Download fact sheet for this course
Cecilia Falkenberg
PhD, Unit Manager Medical Writing & Regulatory Affairs, TFS-Lund

Cost
The cost for the course is EURO 375 + VAT when applying one month prior to the date of the course. An application after that date costs EURO 400 + VAT. The price includes morning and afternoon coffee as well as lunch.