The regulations require you to actively manage risks in the manufacture and handling of medicines/medical devices. During an inspection, you need to show how and argue that decisions have been made based on risk-based thinking. We give you the tools to understand both what a risk-based approach can mean in practice and how to carry out and follow up a risk assessment.
Läkemedelsakademin in collaboration with SwedenBIO and members of course have a discount – just click here. notification.
