Medical Writing in Pharmacovigilance - Update your English writing skills - with many practical exercises!
- Definition of key terms and medical concepts
- Scientific, technical or lay language
- Risk management plan: Contents and structure
- Periodic + Development safety update reports: Practical exercises
- How to avoid common errors
This two-day workshop provides an
introduction to medical writing for
pharmacovigilance, as well as insights
into several relevant safety documents.
Participants will learn regulatory require-
ments and how to apply guidelines to
prepare pharmacovigilance documents. In
addition, they will learn important aspects
of writing and interdisciplinary preparation
of pharmacovigilance documents through
practical exercises. Participants will also
learn about style and terminology for
pharmacovigilance documents (for regu-
latory, medical and lay public) and will
receive tips from experts' practical
experience.
The course will be held in English, thus a
good knowledge of the English language
is required. Nevertheless it will also be
possible to pose questions in German.
Termin
| Datum: | 07.07.2016 |
| Ort: | Novotel Frankfurt City Lise-Meitner-Str. 2 -60486 Frankfurt |
| Preis: | 1.690,00 EUR zzgl. MwSt. |
Zielgruppe
This workshop is intended for those who
work in the pharmaceutical industry and
need to prepare regulatory pharmacovigi-
lance documents. Participants who are new
to medical writing should have some basic
knowledge of the drug development pro-
cess, of regulatory documentation and of
pharmacovigilance.
Participants who are occasionally involved
in the preparation of regulatory documents
and who wish to improve their skills, will
also benefit from this workshop.
Kontaktinformationen
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