An Introduction to Risk Evaluation & Mitigation Strategies (REMS)

An Introduction to Risk Evaluation & Mitigation Strategies (REMS) is a conference dedicated to the FDA thinking of which products qualify for a Risk Evaluation and Mitigation Strategies (REMS).

An Introduction to Risk Evaluation & Mitigation Strategies (REMS) covers topics such as:

  • What products qualify for REMS?
  • The background to REMS
  • Discuss their introduction, maintenance and reporting assessments
  • Understand the different categories of REMS
  • Contrast the approach between the US and FDA for a RMP or REMS programme

An Introduction to Risk Evaluation & Mitigation Strategies (REMS) brings together:

  • QA
  • Pharmacovigilance personnel working in safety review and risk assessments
  • EU QP PVs
  • Clinical personnel

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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