Dr Esther Apos completed her Ph.D in Biochemistry in 1992 through the Faculty of Veterinary Science at the University of Melbourne. Over the past twenty years, she has worked in academic and commercial research, pharmaceutical and medical device product development, clinical trials, and regulatory compliance and affairs. Dr Apos has worked with numerous biotech, medical device and cosmetic companies, developing their product documentation and dossier registration.
George Loizou has worked in the pharmaceutical, complimentary medicine, cosmetic, medical device and IVD areas for the past 20 years. George has extensive experience in product development and quality management systems for all medical device and IVD classes, software as a medical device (SaMD) and the respective technical file dossiers (CE, TGA, FDA). He is also a medical device certified lead auditor for Global European Notified Bodies auditing MDD/MDR, MDSAP and ISO 13485.
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