Harmonising the approach to VeDDRA coding workshop

• Dátum:
  streda, 27 november 2013, All day
• Umiestnenie:
  European Medicines Agency, Amsterdam, the Netherlands

The workshop will provide an opportunity for the regulators and industry to gain hands-on experience using VeDDRA to code adverse event reports and to strengthen the harmonised approach for use of VeDDRA coding terminology.

Documents

Agenda - Harmonising the approach to VeDDRA coding workshop - 27 November 2013

Adopted Reference Number: EMA/500544/2012

Presentation - Best practices in VeDDRA coding (Giles Davis)

Presentation - Overview of process for VeDDRA revision (Raquel Gopal)

Case studies - Harmonising the approach to VeDDRA coding workshop - 27 November 2013

Summary of questions discussed and answers provided on VeDDRA coding at the workshop held on 27 November 2013

Reference Number: EMA/804163/2013