Neha Sah

Experienced in accurately translating medical documentation into complaints codes .Safety and aggregate reporting from solicited and unsolicited sources.

Experience of working on Trilogy. Having knowledge of entering safety information in the trilogy and evaluating the safety information for case seriousness and including potential for upgrade/downgrade of FU cases. Sending upfront clarification requests in case of data discrepancy identified in source documents.

Initiating follow up queries using the relevant letter and tracking follow up attempts till the closure of follow up Having keen knowledge about Execute pharmacovigilance safety management process. A combination of case intake, Duplicate search, case entry, Narrative writing, case follow up,case processing of clinical trial,Allergan case, Spontaneous, Discharge summary and all special situation cases and evaluation of reported adverse events from all sources. Thorough knowledge for Post Marketing Surveillance.

Proficient in MedDRA, Medical codding and WHO dictionary, experienced in complying with medical coding guidelines into uniform medical codes. Having knowledge on anatomical therapeutic chemical classification selection of drug code.

Experience in maintaining patients medical documents, lab reports, procedure and diagnosis into universal medical codes to maintain accurate medical records.

Expertise in handling Veeva EDC, Rave classic, query management.

B.Pharm