target group
Scientific employees in the medical technology and pharmaceutical industry as well as for medical/clinical writers and for everyone who carries out regular research and writes scientific texts.
content
Medical writers play a crucial role in forwarding and documenting generated data. The focus is on the documentation of medical or biomedical research. This brings with it fundamental expectations of the authors and of scientific work in general.
The new seminar and the integrated workshop therefore convey aspects of literature searches in order to narrow them down, define exclusion criteria, select relevant hits and assess the quality of data or clinical studies. Creators of scientific texts - be it for publications, clinical evaluations or well-founded marketing - thus have helpful tools at their disposal.
Based on the scientific and current regulatory expectations according to the valid MEDDEV and MDCG guidelines for medical devices, the topics discussed in the workshop will be implemented together in a practical way.
topic overview
- What is Medical Writing?
- Preparation of the plan / protocol (e.g. Clinical Evaluation Plan)
- Carrying out literature searches (Pubmed, Cochrea, etc.)
- Quality of (clinical) data to be evaluated – Evidence Level
- Collect / summarize and cite data (avoidance of plagiarism)
previous knowledge
Not mandatory.
KONTAKT:
Max-Planck-Straße 17, TuttlingenBeruflichen Bildungsstätte Tuttlingen
