Already a DIA Member? Sign in. Not a member? Join.

Iniciar sesión

¿Ha olvidado su ID de usuario? or ¿Ha olvidado su contraseña?

Not a Member?

Create Account and Join

Holiday Inn London Kensington Forum

21 feb 2017 8:00 a.m. - 22 feb 2017 12:00 p.m.

97 Cromwell Road, London, SW7 4DN, United Kingdom

Post-Authorisation Studies

This course offers insight into EU legislation on PASS and PAES. Examples of PAS protocols as well as some examples of classic pitfalls in study conduct will be presented and discussed.

SESSION 2: EU GUIDELINES/REGULATION – ONGOING CHANGE

Session Chair(s)

Michael  Busch-Sørensen

Michael Busch-Sørensen

Board Member

Danish Society for Pharmacoepidemiology, Denmark

  • Clinical Studies (Study types, Risk based approach, Data privacy & verification/validation)
  • Benefit/risk post approval: GVP (PAS & Registries) & Adaptive licensing
  • PAES Scientific guidance
  • Pragmatic compliance with protocols, submissions, reporting etc.

Speaker(s)

Michael  Busch-Sørensen

EU GUIDELINES/REGULATION – ONGOING CHANGE

Michael Busch-Sørensen

Danish Society for Pharmacoepidemiology, Denmark

Board Member

¿Tiene una cuenta?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.