/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: annapareddy https://cdn.slidesharecdn.com/profile-photo-annapareddy-48x48.jpg?cb=1695028853 WORK SUMMARY o Result oriented professional having over 18 plus years of combined experience in pharmaceutical industry include Clinical Research, Drug Development, Safety reporting for Clinical and Post market drugs, as well in community Pharmacy areas with an excellent proficiency of Information Technology skills. o Adverse Events and SAE’s – identification, classification, recording, review, and reporting, as per FDA Forms 3500A, MedWatch, and CIOMS-I Forms, thus to meet FDA & ICH regulatory reporting requirements & also includes timelines for pre and post marketing; for FDA, EMEA and other world wide ICH regions. o Independent supervision of day-to-day Development of internal and ...