Adverse Event Reporting - Online Training Course

Event details

19th July - 3rd August 2011
at your own desk

About the event

Being involved in drug safety and adverse event reporting, you will also be well aware that reporting obligations are becoming more and more stringent and accurate, timely data reporting is key to patient safety. Establishing a risk based programme is an effective method of ensuring regulations are upheld whilst allowing you to prioritise and minimise cost.

Pharma IQ's Adverse Event Reporting Training Course has been developed along with Graeme Ladds, an industry expert with a wealth of experience in the field of pharmacovigilance. We have constructed the course to give you the tools to achieve this  - all at the comfort of your own desk!

Attendee Information

adverse event reporting, pharmacovigilance, regulations, risk, legislation, MHRA, quality assurance, vigilance intelligence