Milos Stojkovic

Safety Process Director at Roche

Speaker

Safety professional, engaged with establishment and monitoring of processes relating to medical devices vigilance and clinical safety oversight.
Pharmacist by training with experience in regulatory compliance and quality principles related to devices good clinical practice, vigilance/post market surveillance and late development of medical devices.
Member of Serbian Institute for Standardisation technical committee on medical devices, mirror to ISO TC 194, acting as a national lead for ISO 14155 GCP and development of ISO 18969 on clinical evaluation.
Chair of MedTech and Pharma Platform working group on PostMarket Surveillance and Vigilance.