Priyanka Runwall Email and Phone Number

Initial assessment/classification of the complaints received from domestic and regulatory market.Handling of ADE complaint including necessary follow up.Receive information on adverse events, perform initial checks required to check validity of the case, search database to prevent duplicate entries, create case file of received drug safety reports in the safety database.Case processing in Argus safety data base of ICSR including Spontaneous case, Regulatory case, Literature case and Clinical cases.Use medical dictionaries and business guidance to code medical history, drugs andadverse events terms.Prepare narratives summarizing the essential details of the case.Work with the client safety departments, Clinical Safety Scientists and Pharmacovigilance Leaders to ensure that the reports are accurately collected, evaluated and data-based.

working on QMS (quality management system). handling of market complaints received from US/Domestic & ROW...

I had been worked there in Qa department as officer post for 1.2 year.I had been worked there to manage the process & procedure as per the cGMP requirement including the SOP s,training,validation process,qualification & others