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14th EudraVigilance Information Day Adverse drug reaction reporting in the EU and highlights of the new pharmacovigilance legislation Event #13529 23 May 2013 European Medicines Agency, London, United
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Start by familiarizing yourself with the purpose and objectives of the event. Understand the topics that will be covered and the intended audience.
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Who needs 14th Eudravigilance Information Day:

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Regulatory professionals working in the pharmaceutical industry who are responsible for pharmacovigilance and drug safety.
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Healthcare professionals, such as doctors, pharmacists, and nurses, who are interested in staying up-to-date with the latest information on drug safety and adverse event reporting.
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Researchers and academics in the field of pharmacology and drug development who want to enhance their knowledge and understanding of pharmacovigilance.
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Patient safety advocates and organizations interested in monitoring and improving the safety of medicinal products.
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The 14th EudraVigilance Information Day is an event organized to bring together stakeholders to discuss developments in pharmacovigilance and the electronic reporting of individual case safety reports (ICSRs) within the European Union.
Pharmaceutical companies, regulatory authorities, healthcare professionals, and other stakeholders involved in pharmacovigilance are required to participate in the 14th EudraVigilance Information Day.
Participants can register for the event through the official website and attend the various sessions and workshops to learn about the latest updates and best practices in pharmacovigilance.
The purpose of the 14th EudraVigilance Information Day is to promote the safe and effective use of medicines by enhancing pharmacovigilance activities and fostering collaboration among stakeholders.
Participants are expected to share their experiences, challenges, and successes in pharmacovigilance, as well as discuss the importance of timely and accurate reporting of adverse drug reactions.
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