European Union regulatory workshop on medication errors

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TitleEuropean Union regulatory workshop on medication errors
Date28/02/2013 - 01/03/2013
LocationEuropean Medicines Agency, London, UK
SummaryThe workshop is organised by the European Union regulatory network and is aimed at raising awareness of this important public-health issue, discussing the new legal requirements for reporting medication errors and developing best practice among stakeholders. Preregistration open until 21/12/2012. Registration closed.

All documents

Name Language First published Last updated
Medication-errors workshop report (English only) 13/05/2013  
Medication-errors workshop - List of participants (English only) 13/05/2013  
Agenda - Medication-errors workshop - Final programme (English only) 30/11/2012 27/02/2013
Medication-errors workshop - Call for expressions of interest (English only) 03/10/2012  
Presentation - Introduction and objectives of the medication-errors workshop (Peter Arlett) (English only) 11/03/2013  
Presentation - Public-health burden of medication errors and how this might be addressed through the European Union pharmacovigilance system (David Cousins) (English only) 11/03/2013  
Presentation - Do we have a common understanding of medication errors? (Jeffrey Aronson, Robin Ferner) (English only) 11/03/2013  
Presentation - CHMP position paper on medication errors in the context of benefit/risk (Andrea Laslop) (English only) 11/03/2013  
Presentation - Evaluation, classification and weighting of medication errors from an industry perspective (Liz Swain) (English only) 11/03/2013  
Presentation - Medication errors in children (Ian Chi Kei Wong) (English only) 11/03/2013  
Presentation - Medication errors: older patients and their caregivers (Denis O’Mahony) (English only) 11/03/2013  
Presentation - Reporting medication errors at national level: what should be reported and to whom (Mick Foy) (English only) 11/03/2013  
Presentation - Reporting experience from national patient-safety organisations (Maria Jose Otero) (English only) 11/03/2013  
Presentation - Guidance to patients and consumers on medication-error reporting (Kaisa Immonen-Charalambous) (English only) 11/03/2013  
Presentation - Discussion of legal consequences of reporting for healthcare professionals (Carlos Maria Romeo-Casabona) (English only) 11/03/2013  
Presentation - Operational definition of medication error for European Union reporting requirements (Thomas Goedecke) (English only) 11/03/2013  
Presentation - Good practice: Medical Dictionary for Regulatory Activities coding of case reports resulting in harm (Sabine Brosch) (English only) 11/03/2013  
Presentation - Spontaneous reporting: detecting medication errors and suitability of current systems (Phil Tregunno) (English only) 11/03/2013  
Presentation - Identification of preventable adverse drug reactions from a regulatory perspective (Almath Spooner) (English only) 11/03/2013  
Presentation - Root-cause analysis in context of World Health Organization international classification for patient safety (David Cousins) (English only) 11/03/2013  
Presentation - Medication names and medication errors (Annemarie Hellebek) (English only) 11/03/2013  
Presentation - A re-design evaluation from the real world (Annemarie Hellebek) (English only) 11/03/2013  
Presentation - Regulatory tools for managing the risk of medication errors: labelling and patient information (Jan MacDonald) (English only) 11/03/2013  
Presentation - Minimising harm through education (Tony West) (English only) 11/03/2013  
Presentation - Medication errors: development of prevention strategies for medicines and medical devices (Laurent Auclert) (English only) 11/03/2013  
Presentation - Regulatory tools for risk minimisation and their effectiveness: monitoring health outcomes and patient compliance (Sabine Straus) (English only) 11/03/2013  
Presentation - Best-practice communication for healthcare professionals and patients (Angeles Alonso-Garcia) (English only) 11/03/2013  
Presentation - Implementation report on the patient safety recommendation 2009/C151/01 (Directorate General for Health and Consumers) (English only) 11/03/2013  
Presentation - Adverse reactions from medication errors: regulatory experience in European Union (Dolores Montero) (English only) 11/03/2013  
Presentation - Medication errors: what patients can do to minimise them (Francois Houyez) (English only) 11/03/2013  
Presentation - Medication errors: FDA perspective (Carol Holquist) (English only) 11/03/2013  
Presentation - Medication-errors workshop: Closing remarks (Peter Arlett) (English only) 11/03/2013  

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