<ul><li>Ensuring that all output complies with the European Medicines Evaluation Agency (EMEA) regulations, Dutch codes of practice and license conditions where necessary.</li><li>Overseeing medical premarket approval of new chemical entities (NCEs).</li><li>Identifying study-related regulatory and quality issues, and managing complaints and any subsequent legal actions.</li><li>Designing and implementing campaigns such as those for disease awareness and medical education, depending on the organisation’s products.</li><li>Participating in meetings with senior management and attending external meetings and congresses on behalf of the company.</li><li>Developing the best possible working relationships between the organisation and stakeholders, especially key opinion leaders.</li></ul>

Medical Affairs