Milica Talic

Background

About Milica Talic

With 30 years’ experience in quality assurance, clinical and regulatory affairs in the medical devices industry, I provide trusted consultation to executive teams on matters impacting global operations and growth. Galvanising internationally teams to deliver challenging regulatory, quality and clinical projects, including major transitions aligning with shifts in regional distribution models, I balance the need for absolute integrity in the management of regulatory and clinical affairs with evolving commercial priorities. Skilled in protecting business growth and ongoing profitability, I use an expert understanding of international regulatory regimes (APAC, ANZ & Europe) and relationships across the industry to ensure the proactive management of regulatory functions. A natural leader and mentor, I enjoy building leadership bench strength within teams. Having established teams and scaled functions at a regional level, my mission is to build regulatory capabilities, teams and frameworks that are ultimately self-sustaining. My aim is always to share knowledge and empower others to deliver their best, building a culture of collaboration and transparency to work towards the delivery of shared goals. I welcome new connections within the business community. Please feel free to get in contact through LinkedIn. Specialities: Regulatory Affairs (TGA, FDA and other global regulatory bodies), Quality Assurance, Clinical Affairs, Program Management, Business Growth & Transformation, Risk Management & Compliance, C-suite Advisory, Leadership Development, APAC, Europe, ANZ, USA.