Follow the journey of a medicine for human use assessed by EMA in this interactive timeline. EMA’s human medicines committee (CHMP) has completed its rigorous evaluation of Comirnaty, concluding by consensus that sufficiently robust data on the quality, safety and efficacy of the vaccine are now available to recommend a formal conditional marketing authorisation. European Medicines Agency - EMA organises a second public meeting about the new COVID-19 vaccines. It particularly concerns the centralised procedure, where the European Medicines Agency (EMA) plays a key role. Masters degree in international drug development and registration, Head of Advanced Therapies, European Medicines Agency (2020-present), Head of Specialised Scientific Disciplines, European Medicines Agency (2013-2020), Head of Risk Management, European Medicines Agency (2012-2013), Head of Risk Management (ad interim), European Medicines Agency (2011-2012), Head of Signal Detection and Data Analysis, European Medicines Agency (2009-2011), Scientific Administrator, European Medicines Agency (2003-2009), Medical Editor, EuroTransmed, United Kingdom (1998-2003), Scientific Project Manager, Medical Action Communications, United Kingdom (1997-1998), Post-doctoral Researcher, Clinical Research Centre, United Kingdom (1995-1996). Doctor of Philosophy in molecular and cell biology, Head of Labeling, European Medicines Agency (2020-present), Head of Labeling Review and Standards Office, European Medicines Agency (2014-2020), Responsible for the Quality Review of Documents Group Secretariat, European Medicines Agency (2004-2009), Administrator, European Medicines Agency (2001-2004), Research Assistant, Ministry of Interior and Public Administration, Athens, Greece (1994-1995). This may be as a result of a planned downtime for maintenance. The Division maintains close contact with other decision-makers in healthcare and with international partners, in conjunction with the Agency's international-affairs function. Withdrawal of the eAF v1.23.1.3, v1.23.1.4 Variation, Renewal and MAA (human and veterinary) forms from the eAF website however, the forms are accepted by the EMA and NCAs until 31.12.20. The European Medicines Agency's (EMA) Human Medicines Division oversees human medicines throughout their lifecycle. EMA’s human medicines committee (CHMP) has completed its rigorous evaluation of Comirnaty, concluding by consensus that sufficiently robust data on the quality, safety and efficacy of the vaccine are now available to recommend a formal conditional marketing authorisation. EMA Pharmaceuticals presents SMARTSEAL, a powerful covert anti-counterfeiting feature, enabling the easy track & trace of the individual container through RFID technology. The entry pages on these topics provide an overview of the topic and direct users to relevant content in the product lifecycle sections. EMA Pharmaceuticals presents SMARTSEAL. The EMA is … Its day-to-day operations are carried out by the EMA staff, overseen by EMA's Executive Director. Emergency Medical Associates is a physician-led, privately held physician management company that specializes in emergency and hospitalist medicine. If the site still contains content that does not yet reflect the withdrawal of the UK from the EU, this is unintentional and will be addressed. The Division supports the work of the European medicines regulatory network to produce high-quality patient-centred scientific evaluations and in ensuring compliance with good-practice standards. Master's degree in European regulatory affairs, Head of Meeting Secretariat, European Medicines Agency (2020-present), Head of Working Parties Secretariat (ad interim), European Medicines Agency (2015-2020), Scientific Administrator, European Medicines Agency (2009-2015), Regulatory Affairs Manager, Schering-Plough, Brussels, Belgium (2006-2009), Regulatory Affairs Officer, Baxter, Brussels, Belgium (2003-2006), Trainee, Baxter, Nivelles, Belgium (2003), Deputy Head of Packaging, Schering AG, Lys-lez-Lannoy, France (2000-2003), Deputy Head of Packaging, Laboratoires UPSA, Agen, France (1997-2000), Project team manager, Laboratoires UPSA, Agen, France (1995-1997), Trainee, Laboratoires UPSA, Agen, France (1994-1995), Trainee, Roussel-Uclaf, Paris, France (1991-1992), Hospital pharmacy trainee, Central University Hospitals, Nancy, France (1990-1991), Masters in regulatory affairs and health economy, University of Lille/Paris/Lyon, France (2003), Masters in pharmaceutical manufacturing, University of Bordeaux, France (1994), Doctor of pharmacy specialising in industry, University of Nancy/Bordeaux, France (1996), Head of Procedures, European Medicines Agency (2020-present), Head of Evaluation Procedures D, European Medicines Agency (2014-2020), Scientific Administrator, European Medicines Agency (2006-2014), Business Intelligence Analyst, AstraZeneca, Madrid, Spain (2004-2006), Master in management of pharmaceutical and healthcare industries, Instituto de Empresa, Madrid, Spain (2004). 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