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Session Chair(s)
Sinisa Tomic, PHD
Head of Agency
Croatian Agency for Medicinal Products and Medical Devices, Croatia
Learning Objective : Participants will learn about the placement of medical devices in croatia in the pre-accession period. Furthermore, they will learn about the harmonisation process of the national legislation and the transposition of new approach directives.
Speaker(s)
Latest News from the International Medical Device Regulators Forum and Future Goals: IMDRF
Mike Ward
World Health Organization (WHO), Switzerland
Coordinator, Regulatory Systems Strengthening, EMP
How Industry Is Working to Make its Voice and Priorities Heard at the Global Regulatory Level
Sabina Hoekstra-van den Bosch, PHARMD, MSC, RPH
Tüv Süd, Netherlands
Global Director Regulatory Strategy
Regulating Medical Devices in the Pre-Accession Period
Sinisa Tomic, PHD
Croatian Agency for Medicinal Products and Medical Devices, Croatia
Head of Agency