About the UMC
The WHO set up its International Drug Monitoring Programme after the thalidomide disaster. Since 1978 the Programme has been carried out by the Uppsala Monitoring Centre (UMC) in Sweden.
An independent centre of scientific excellence, the Uppsala Monitoring Centre is responsible for the collection of data about adverse drug reactions from around the world, especially from countries that are members of the WHO, and the generation of signals of drugs which might possibly have problematic side-effects.
Through a range of products and services, derived from the WHO database, the UMC provides essential resources for regulatory agencies, health professionals, researchers, the pharmaceutical industry and prescribing physicians.
Public holidays: please note that the Uppsala Monitoring Centre will be closed on the following holidays in Uppsala: 2, 5 and 30 April, 13 and 14 May and 25 June 2010.
[Top of page]
Vision
'UMC improves worldwide patient safety and welfare by reducing the risk of medicines'
Mission statement
The purpose of the UMC is to be recognised world wide as:
- a global centre of scientific excellence committed specifically to the reduction of risk in medication and to the safeguarding of patient health and welfare
- a leader in the research and development of tools and methodologies for pharmacovigilance and patient safety
- a prime resource for all stakeholders involved in international collection, coding, assessment, analysis, interpretation and communication of data relating to drug safety issues and patient safety concerns
- a preferred provider of high quality and cost-effective international drug and medical dictionaries, classifications, and terminologies
- an organisation with open, impartial and ethical values and performance.
Values
The underpinning aspirational value of UMC is to give service to the people of the world, especially patients, and all those who work for their safety and wellbeing. The corporate tag-line 'Safeguarding patients' reflects an extension of the previously known focus of the UMC relating to drug safety towards the end beneficiary. Below are the operational values guiding us in our daily work and in all collaborations. We will:
- provide innovation and leadership in the area of patient safety
- conduct our operations within WHO principles and concepts
- constantly develop our knowledge and strive for scientific excellence
- deliver high quality products and services to all our customers
- always have a global focus, particularly considering the needs of developing and emerging countries
- seek and maintain active and fruitful collaboration with all stakeholders
- actively listen to all partners' views whilst maintaining the highest possible level of integrity and impartiality
- favour openness and transparency in our communications without sacrificing confidentiality and data security needs
- encourage creativity and intellectual adventurousness, amongst UMC staff and in our relationships
- endeavour to earn trust and respect, by applying the highest ethical and technical standards in everything we do
- defend the position of the UMC as a unique organisation, balancing income-generation and the public good in its products and services.
[Top of page]
Annual report July 2008 - June 2009The latest Annual Report (2008-2009) (pdf) describing the Uppsala Monitoring Centre's activities is available here for viewing/download.
[Top of page]
UMC Board of DirectorsThe operations of the WHO Collaborating Centre (UMC) are governed by an agreement between WHO Headquarters and the Swedish government. The Centre has an international Board where WHO appoints three members and three others are appointed by the Swedish government.
Chairman of the Board is Mr Carl Älfvåg, Director-General, Swedish Agency for Disability Policy Coordination. His deputy is Assistant Professor Ellen Vinge, clinical pharmacologist, University of Lund.
The other members appointed by the Swedish Government are Anders Rane, professor of clinical pharmacology (alternate Professor Ulf Bergman) both at the Karolinska Institute, Stockholm and Ms Marianne Dicander Alexandersson, Apoteket AB (alternate Ms Ingela Tuvegran, director at Södra Älvsborg Hospital, Borås).
WHO has appointed Dr Lembit Rägo (alternate Dr Mary Couper) from WHO headquarters, Dr June Raine from the UK's MHRA (alternate Dr Norbert Paeschke from the German Drug Control Agency, BfArM), and Professor Mohammed Hassar (alternate Dr Rachida Soulaymani-Bencheikh) from the Moroccan Institute of Hygiene.
[Top of page]
UMC Staff

Director Marie Lindquist PhD, MSc Pharm, Dr Med Sc
Finance and Core ServicesBirgitta Toreheim CA, Manager, Chief Financial Officer Ali Bahceci Network Technician Britt Gustavsson-McCurdy, Corporate Secretary Anneli Lennartsson Economy Assistant Anette Sahlin Administration Assistant
Safety Support & Services Monica Plöen BSc Pharm, Manager Cecilia Biriell MSc Pharm, Senior Specialist, WHO-ART Carin Ellene MSc Pharm, WHO Drug Dictionaries Content Management Mohamed H Farah Pharm D, Senior Specialist, Traditional Medicines Sara-Lisa Fors BSc Pharm, Safety Reporting Richard Hill BSc, MBBS, Medical Assessor Malin Jakobsson, MSc Pharm, WHO Drug Dictionaries Content Management Jeanette Johansson BA, BSc Pharm, Review Panel Co-ordinator Helena Sköld MSc Pharm, Signal Detection Elki Sollenbring MSc Pharm, WHO Drug Dictionaries Traditional Medicines Lovisa Sällstedt MSc Pharm, Safety Reporting Anders Viklund MSc Pharm, Information Retrieval Camilla Westerberg BSc Pharm, WHO Drug Dictionaries Content Management Helena Wilmar BSc Pharm, Team Leader: Safety Reporting Malin Zaar Pharmacist, Team Leader: WHO Drug Dictionaries Content Management
External Affairs Sten Olsson MSc Pharm, Manager, Chief WHO Programme Officer Geoffrey Bowring BA, External Affairs Co-ordinator Anna Celén MSc Pharm, External Affairs Pharmacist (on parental leave) Jerry Labadie MD, Vaccine Safety Specialist
Marketing Annika Wallström MSc Pharm, Manager, Chief Marketing Officer Jessica Avasol, Sales and Marketing Assistant Sara Bergh, Sales Assistant Hannah Björn, Marketing Assistant Katarina Hansson, Senior Sales and Marketing Assistant Carl Huddénius MSc Pharm, Assistant Product Manager Anna Mattsson BSc Pharm, Support Executive Mats Persson BA, Manager, Head of Sales and Marketing Henrik Sahl, Sales Support Manager Ola Strandberg MSc, Vendor Liaison Officer Daniel von Sydow MSc Pharm, Product Manager
Research Niklas Norén PhD, Manager Tomas Bergvall MSc, Research Engineer Ola Caster MSc, Drug Safety Analyst Johan Hopstadius, MSc Eng Phys, Research Engineer Kristina Star RN, BMedSc, Drug Safety Analyst Johanna Strandell MSc Pharm, Drug Safety Analyst
Production, Development and Quality Johanna Eriksson, Manager Bill Dagérus, Senior Systems Developer Stefan Lewenfalk, Senior Systems Developer Annica Lundström BSc Pharm, Quality Co-ordinator Nike Meder Pharmacist, Production Leader Bjorn Moberg, Systems Developer Jessica Nilsson BSc Pharm, Team Leader: ICSR database Sven Purbe BA, Senior Specialist Ulrika Rydberg BSc Biol, PhLic, Quality Co-ordinator Shalini George Tharakan MSc, Systems Developer Thomas Vidinghoff MSc, Senior Systems Developer Magnus Wallberg MSc Eng Phys, Senior Systems Architect Bo Östling, Senior Systems Developer
Medical Advisor Ralph Edwards MB, ChB, FRCP (Lond), FRACP
[Top of page]
Signal review panelFor over fifteen years the UMC has been fortunate to have the assistance of volunteer consultants as 'signal reviewers'. These clinical experts review the results of the regular computerised screenings of ADR reports submitted to the WHO Programme. The results of their work, consisting of a summary of available evidence, are circulated to national pharmacovigilance centres periodically in the 'SIGNAL' document.
Signal reviewers held a meeting in October 2008 in Uppsala (a report appeared in Uppsala Reports 44, January 2009).
During the review panel meeting in 2000, a proposed 'signal detection worksheet', useful when analysing case reports, was discussed and finalised. This worksheet is available for viewing/download > Signal detection worksheet.
For information on the reviewers, click on their names below (full information on all reviewers not available at present):
|
Dr Ariel E Arias, Canada Dr Joanne Barnes, New Zealand Ms Anna-Lena Berggren, Sweden Mr Maximiliano Bergman, Argentina Prof Gunnar Boman, Sweden Dr Ian Boyd, Australia Dra Mabel Burger, Uruguay Prof Alfonso Carvajal, Spain Dr David W J Clark, New Zealand Dr Anita Conforti, Italy Dr Ana Maria Corrêa Nunes, Portugal Prof Dr Andrew Czeizel, Hungary Prof Richard Day, Australia Prof Peter de Smet, Netherlands Dr P Murali Doraiswamy, USA Prof Edzard Ernst, United Kingdom Dr Rick Fraunfelder, USA Ms Birgitta Grundmark, Sweden Dr Pär Hallberg, Sweden Dr Kenneth Hartigan-Go, Philippines Dr Staffan Hägg, Sweden Prof Peter Jacobs, South Africa Dr Sylvia Kardaun, Netherlands Ms Anne Kiuru, Sweden Prof Milan Kriska, Slovakia |
|
Dr Nilima Kshirsagar, India Prof Michael Langman, United Kingdom Prof P O Lundberg, Sweden Dr Jens Lundgren, Denmark Dr M Laurie Mashford, Australia Dr John McEwen, Australia Dr Ronald H B Meyboom, Netherlands Dr Ed Napke, Canada Prof Tamás L Paál, Hungary Dr Martin Pfeiffer, Germany Dr Robert Pless, Canada Dr Alain Rohan, USA Dr Emilio J Sanz, Spain Dr Ruth Savage, New Zealand Dr Saad Shakir, United Kingdom Dr Debbie Shaw, United Kingdom Mr Ivan Stockley, United Kingdom Dr Michael Tatley, New Zealand Dr Mary Teeling, Ireland Dr Ingrid Trolin, Sweden Prof Kiichiro Tsutani, Japan Prof Giampaolo Velo, Italy Dr Anthony Wong, Brazil Dr Qun-Ying Yue, Sweden | |