Successful Medical Writing – from Protocol to CTD
Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals. This process largely relies on the quality of documentation submitted to the regulatory authorities, and a high standard of medical writing plays a vital role in ensuring a positive outcome. This intensive three-day medical writing course will help you to improve your skills and achieve this standard.
Aims and objectives
This event combines presentations from our expert faculty with practical exercises to provide a thorough introduction to the basics of medical writing that goes beyond the usual ‘overview’ courses. It will provide in-depth training in general writing and data presentation skills, and specifically in the kind of documents most frequently encountered in clinical research.
You will learn both the theoretical and practical aspects of writing for regulatory authorities as well as the sensible use of international guidelines, standards and useful writing tips. Many illustrative examples will be used, drawn from the course leaders’ wide experience of the pharmaceutical industry.
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Reviews by course attendees
Average rating 4.5
The content was targeted, appropriate and informative. Presentations were good, incorporating both text and visual elements to keep us engaged, and the speakers were friendly an...
The content for each day was great and very informative, as a new starter to the industry it really helped me to gain an understanding of the layout, structure and what to look ...
Overall, I found the webinar interesting and worthwhile. The speakers were all highly knowledgable and gave good advice. I believe this webinar is suitable for beginner medical ...