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European Medicines Agency

Apr 29, 2014 8:00 AM - Apr 29, 2014 5:00 PM

30 Churchill Place, Canary Wharf, London, E14 5EU, United Kingdom

2nd Periodic Safety Update Report Information Day

Session 1 - 1

Session Chair(s)

Heidi  Janssen

Heidi Janssen

Head, Endocrinology, Metabolism & Cardiovascular

European Medicines Agency, Netherlands

Irene  Rager

Irene Rager

Head of Service E, Procedure Management Department

European Medicines Agency, Netherlands

This session will provide a detailed update on the technical and procedural aspects in relation to PSUR submissions and the PSUR single assessment. It will start with an overview of the PSUR/PSUSA assessed so far including statistics, type of outcome and challenges encountered. Other key areas addressed will include procedural aspects related to periodicity, submissions and the maintenance of the EURD list. The PSUR repository functionalities to be audited will be also summarised.

Speaker(s)

Maria  Boulos

An overview of the PSUR/PSUSA assessment experience so far

Maria Boulos

European Medicines Agency, Netherlands

Scientific Administrator

Katerina-Christina  Deli

Application of the EU reference date list for PSUR submissions

Katerina-Christina Deli

European Medicines Agency, Netherlands

Ana  Zanoletty Perez

Submission requirements and procedural aspects of the PSUR single assessment procedure

Ana Zanoletty Perez

European Medicines Agency, Netherlands

Head of Clinical Trials Transformation Workstream

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