My expertise and experience have been instrumental in my contribution in the development of the research sector in Mauritius. Having worked in one of the leading global organisations in clinical trials, upon my relocation to Mauritius, I have set up the framework for registration of Contract Research Organisations, drafted regulations for Clinical Trials on medical devices, national guidelines for the Clinical Trials sector, regulations for pre-clinical trials, regulations of the Mauritius Diaspora Scheme and facilitated implementation of same. Through the MIBL, I am now driving the research and biotech sector to new heights. The research industry has to be overseen in a non-sporadic way and my role at MIBL allows me to act as interface between government, investors, academia, incubators and international partners to have a productive output meeting our national priorities.