Summary
This agency is responsible for the evaluation, supervision, and safety monitoring of medicines within the European Union. It engages in various activities including marketing authorization, post-authorization processes, and regulatory oversight for both human and veterinary medicines. The agency collaborates with healthcare professionals, patients, and the pharmaceutical industry to ensure the efficacy and safety of medicinal products.
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2009 |
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2010 |
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2011 |
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2012 |
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2013 |
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2014 |
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2015 |
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2016 |
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2017 |
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2018 |
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2019 |
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2020 |
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2021 |
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2022 |
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2023 |
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2024 |
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