Quality Documents & Training Coordinator
Global PV Quality
She is a qualified professional in Pharmacovigilance and Regulatory Affairs areas. she studied Pharmaceutical Sciences at Faculdade de Farmácia da Universidade de Lisboa (Faculty of Pharmacy of Lisbon University) (high degree) and concluded three postgraduate studies in Epidemiology, Economic Evaluation of Medicines and Statistics Applied to Health (e-learning) at Faculdade de Medicina da Universidade de Lisboa (Faculty of Medicine of Lisbon University), Lisbon School of Economics and Management (ISEG) and IHMT/Universidade Nova de Lisboa, respectively. I also received education on quality by Ordem dos Farmacêuticos (the Portuguese Association for Pharmacists) and I’m a qualified trainer. she got her practical professional experience mainly at consulting companies, firstly as a regulatory affairs officer and afterwards as pharmacovigilance manager, where she contacted with different pharmaceutical companies and multiple requirements. she is currently working at a pharmaceutical company in Czech Republic as a Quality Documents & Training Coordinator. Her experience in the pharmacovigilance area includes the setting up and maintenance of pharmacovigilance systems in national and multinational pharmaceutical companies within Europe for post-market drugs. Additionally, she worked as a technical director in a pharmaceutical company, where I was responsible for the warehouse compliance with the legislation in place, the preparation of Good Distribution Practice manual, the management of the registration documents to Competent Authorities, and the carrying out of all the subsequent discussions necessary to maintain marketing authorisations for the products concerned, participating in the resolution of production and quality control problems related to the marketing authorisations.