The EU GVP modules have been in place for almost 4 years now and there have already been a couple of updates to individual modules. This webinar will briefly take you through
This webinar covers the legislation around device vigilance and helps you understand what needs to be reported and how this differs from reporting for medicinal products.
With the updated EU legislation there are more definitive requirements for post authorisation safety studies. Understand the definitions and what your obligations are. This
As the EU has started to monitor marketing literature, now is a good time to revisit your literature and ensure it is compliant for the regulators; this includes reviewing for
Join Dr. Seema Jaitly on her latest webinar which will look into signal detection in more detail. Great for those who are new to pharmacovigilance or embarking on signal
A large and time consuming part of your role will no doubt include writing detailed reports which face the scrutiny of the regulators. This short webinar being run by Dr Seema
Risk Minimisation isn’t a new concept in pharmacovigilance yet it is rapidly evolving and it can be hard to stay on top of all the latest guidelines and developments.