This course provide brief overview of national, mutual recognition / decentralized and centralized procedures along with timeline flowcharts. It also touch base upon accelerated review, conditional approval and exceptional circumstances. This course is beneficial for regulatory affairs, quality assurance, R&Dprofessionals who would like to start their career in European (EU) healthcare or pharmaceutical market. With this course professionals will be able to understand different types of EU marketing authorization procedures along with their legal basis, conditions and pre-requisites which will help professionals in building robust regulatory strategies for quick market penetration and medicinal product launch.