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Lovisa Sällstedt, MSc Pharm, Safety Reporting
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Provides support to member countries of the WHO Programme for International Drug Monitoring on ICSR (Individual Case Safety Report) related issues, including support and training on VigiFlow.
Involved in the overall process and quality evaluation of ICSRs submitted to the WHO Global ICSR database (VigiBase).
Also involved in the development and quality assurance of VigiBase, VigiFlow and PaniFlow.
Contact person for companies using VigiFlow.
E-mail: lovisa.sallstedt@who-umc.org |
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Lovisa Sällstedt page last updated 17 November 2009