... all Adverse Event Reports occurring in patients which are taking or have previously taken the manufacturer’s product. Submit all adverse event reports to manufacturer/third party vendor within ...

... . Responsible for the identification, intake, documentation, and submission of all Adverse Event Reports ... adverse event reports to manufacturer/third party vendor within stipulated timeframe; additionally follow ...

... . Responsible for the identification, intake, documentation, and submission of all Adverse Event Reports ... adverse event reports to manufacturer/third party vendor within stipulated timeframe; additionally follow ...