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Regulatory affairs & scientific relations
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EMA is the European Union agency responsible for:</p><ul> <li>Evaluating the efficacy and safety of medicines submitted for EU marketing authorization</li> <li>Monitoring safety across the lifecycle of medicines</li> </ul><p>We've built a strong, mutually beneficial relationship with EMA that encompasses:</p><ul> <li>The exchange of information and advice</li> <li>Joint educational activities</li> <li>The nomination of experts for regulatory assessment and scientific consultations</li> </ul><p>Our relationship also encourages dialogue between regulators and medical experts on a range of issues, including:</p><ul> <li>Emerging trends and issues arising from scientific and technological innovation</li> <li>The implications of new EU legislation</li> </ul><p>EHA actively participates in several EMA groups and platforms, including the:</p><ul> <li>Health Care Professionals Working Party (HCPWP)</li> <li>Policy Officers Group (HCP POG)</li> <li>Cancer Medicines Forum</li> <li>ACT EU Multi-stakeholder Platform Advisory Group (MSP AG)</li> </ul><p>We also interact and collaborate with relevant EMA expert teams and groups, such as:</p><ul> <li>Haematology Working Party (HaemWP)</li> <li>Inter-Committee Scientific Advisory Group on Oncology</li> <li>ATMPs & Haematology Office</li> <li>Committee on Advanced Therapies (CAT)</li> <li>Committee on Orphan Medicinal Products (COMP)</li> </ul><p>Read our monthly news and updates on EMA scientific committees' decisions and hematological medicines on the <a href="/advocacy/selected-ema-news/">selected EMA news page</a>.</p><h2>Scientific relations</h2><p>European Affairs closely interacts with EHA’s Specialized Working Groups (SWGs). 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