The main role of medical writers is to create well written
documents and manuscripts as per standard formats, compliant to regulatory
standards for approval of new clinical trials, drugs, medical devices and
biologics.
Upon completion of this course, participants will gain the
foundational knowledge and skills for a proper medical and technical writing in
the regulated environment.
- Medical doctors and other health care
personnel involved in medical research
- Graduate degrees in biomedical or life sciences, such as
biology, chemistry,
pharmacy, nursing, nutrition, medicine or public health.
- Understand
the overall process of research and the structure of an article
- Differentiate
between the different study designs used in clinical research
- Gain
further understanding of the basics of statistics in medicine
- Understand
the different biases that affect clinical research
- Apply
the principles of EMB in clinical practice
- Understand
the critical appraisal process
