Lara Shamon Email & Phone Number

Stockholms Län, Sverige

Medical Information: handling of all received medical Information inquiries and provide accurate, balanced, and scientifically valid information in response to inquiries regarding marketed and investigational products. Pharmacovigilance;as a Local PV manager my role is to ensure that all potential adverse drug reactions received are identified and.

My main task was to validate and classify drug information from various international sources into WHODrug Global, including validating trade names, MAH information, substances, and ATC assignments. I also performed changes to already existing entries in WHODrug to meet customer needs and coding conventions and code Individual Case Safety Reports (ICSRs).

Stockholm, Sverige

My main tasks were divided into pharmacovigilance and quality assurance. As a Pharmacovigilance Officer I was responsible for all incoming Adverse Events, Medical Device Incidents (diabetic and non-diabetic products), medical information request and reconciliations with different companies. The different reports were registered in the company internal.

Uppsala, Uppsala Län, Sverige

My main task was handling the adverse event reports that are submitted to the Medical Products Agency from both consumers and healthcare professionals.The handling of these reports is done by first ensuring that the report is valid and if the requirements are met, the report is then registered. The reported terms need to be coded, and MedDra is the coding.

Uppsala Län, Sverige

Uppsala, Uppsala Län, Sverige

Enköping, Uppsala Län, Sverige