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The purpose of the SEaL System is to share, for learning purposes, across the European Union
- patient safety issues identified within Member States and
- identified patient safety initiatives
The mechanism will facilitate the sharing of information identified within Member States with other Member States.
The mechanism is a voluntary one, from putting information into the mechanism through to accessing and acting upon the information within it. There are no legal requirements for Member States to interact with the mechanism or to implement the details within the reports on the mechanism. The System is not linked to existing EU mandatory reporting systems on pharmaceutical and medical devices.
The patient safety issue or solution submitted to the system has been identified and developed in the context of that Member State’s healthcare environment. The applicability to other healthcare environments has not been assessed and it is the responsibility of those who access the patient safety issue or solution to ensure that a full risk and impact assessment has been made of the solution before implementing any of the solutions.
Subscribers are notified that a new entry has been made and can then access the information of the report. Select the menu subscribe and fill out the form.
Below are the last SEaL notifications that have been sent to the system.
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Latest reports:
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