>Signal Management:Monitoring continuously all available data due to identification of safety issues.Conducting signal detection processes for each company medical productProcessing and managing potential signals from EVDAS EMA.>Supported Marketing OTC Department:-Composing new herbal compositions as line extension-Searching for new potentials for herbal products and supplements- On the basis of these projects, new products from cardiology and urology area were created and brought into life.>In house SMQ MedDRA tool training.

>Processing case related information including interpretation of medical conditions, lab results procedures and concomitant drugs>Was engaged in department Standard Operating Procedures creating. Ensured compliance with corporate and department Standard Operating Procedures.>New team members training

>Benefit-Risk Assessment (BRA) documents writing>Performing timely and accurate triage of adverse event reports including Individual Case Safety Reports, complains and inquiries from physicians, pharmacies, consumers and sales representatives. >Reviewing ad completing all safety information communicated spontaneously and from literature on assigned products in accordance with drug safety guidelines and pharmacovigilance regulations.>Providing medical evaluation of adverse reactions and serious adverse event reports from initial and follow up source documents for clinical accuracy and consistency including narrative, medical coding using MedDRA, seriousness, expectedness causality assessment.

>Performing activities relating to collection, processing, follow up, analysis of adverse reactions and serious events for extended number of products.>Reviewing worldwide literature an weekly basis.

>Analysing and processig of medical cases ( ICSRs)