I am a Pharmaceutical scientist, my working experience includes clinical researcher in R&D and QA in pharmaceutical companies. I am expertise in pharmaceutical and medical device regulatory activities, I holds Masters in medical device regulatory affairs and Masters in Pharmaceutical technology, from University College Dublin. I was carried out numerous research projects on various aspects of clinical research and regulatory compliance. My current research interests include the in-vitro diagnostic kits (IVDR) and regulatory requirements, the clinical trials in cancer research and development, the primary focus is on the non-accuracy of the diagnostic tests, also the regulatory gaps in the developing countries and the rapidly evolving filed of OSNA device for solid tumour biopsies to guide therapeutic decision (particularly Breast Cancer). Currently I am in R&D for clinical and transnational research trials at St Peter’s Hospital, UK.