Clinical Trials in Rare Diseases MasterClass

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The focus of this two days training will be on providing an update of ongoing activities regarding medicines’ risk and signal management. The first day will be an opportunity to provide the participants with practical advice on RMP drafting and preparation as well as the accessor’s point of view in evaluating an RMP.

The participants will have the opportunity to get an insight on the current signal detection and management guidelines and tools. What are the authorities’ expectations and findings in the signal management area? During the signal management session, pragmatic approaches, real-life examples, lessons learned, as also processes for signal management and eRMR assessment will be discussed.

During this training, an outlook of the interactions between Drug Safety and other internal (e.g. Regulatory Affairs) and external stakeholders (health Authorities) will be given. How we communicate efficiently signals, Emerging safety issues (ESISs), and other safety communications (i.e. DHPCs) will be discussed.

For price and detailed agenda, visit the website and request the agenda!

Language: english

Price: Free