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