Scientific Writing and Reviewing in Regulatory Affairs - Update your English writing skills!
- Free writing versus regulatory restrictions
- Writing and reviewing regulatory documents
- Editing and proofreading documents
- Package leaflet - regulatory linguistic restrictions and user-friendly writing
- Good writing skills - example: clinical overviews and summaries
After completing this seminar, participants
will be aware of the key regulatory
requirements when preparing texts, with
a greater awareness of the importance
of proper English writing, reviewing and
proofreading processes.
Practical examples regarding the English
wording in package leaflets and clinical
overviews and summaries complete this
seminar.
Termin
| Datum: | 27.04.2015 |
| Ort: | relexa hotel Lurgiallee 2 -60439 Frankfurt |
| Preis: | 1.390,00 EUR zzgl. MwSt. |
Zielgruppe
This seminar is intended for all those
working in regulatory departments in the
human and veterinary pharmaceutical
and medical device industries with basic
experience in writing, reviewing or
proofreading regulatory documents in
English.
Participants should have good English
reading and writing skills and a basic
knowledge of regulatory documentation.
Kontaktinformationen
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