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Medical Writing

02-12-2015 - 16:00 - 18:00

Dette er det 3. og sidste planlagte medlemsmøde i rækken af møder omkring data håndtering. Tidligere i år har der været afholdt møder om data management og statistik.

At this meeting, you will be introduced to the world of medical writing, which encompasses much more than the clinical trial report. You will hear about the various contributions that medical writers provide in the different phases of clinical development. You will gain insight into how the huge amount of documentation produced at clinical sites as part of a clinical trial is compiled into a well-structured, cross linked output for submission to health authorities. You will learn how the new clinical trials regulation has implications for the medical writing discipline. And you will receive an introduction to publication medical writing and publication ethics, including the recently updated Good Publication Practice guideline (GPP3).

Programme:
16.00 – 16.10   Welcome

16.10 – 16.20   Introduction to Medical Writing
by Carsten Roepstorff, Director, Science & Medical Writing, Larix A/S

16.20 – 16.50   Medical Writing of Regulatory Documents
by Jeff Craven, Senior Medical Writer, Larix A/S

16:50 – 17:20  Break / Networking (sandwiches will be served)

17:20 – 17:50   Publication Medical Writing
by Angela Stocks, Principal Medical Writer, Larix A/S

17:50 – 18:00     Additional questions and wrap-up

Bemærk endvidere også, at dette medlemsmøde vil foregå på engelsk.

Med venlig hilsen
Bestyrelsen for Dansk Selskab for Good Clinical Practice

 

Se præsentationerne fra mødet her:

Medical Writing

Detaljer

Dato:
02-12-2015
Tidspunkt:
16:00 - 18:00

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