A Legal Framework for Population-Based Cancer Registries
Digital Tools
Cancer Registries
IARC announces the print availability of a toolkit designed to support countries in establishing the legal basis for mandatory reporting of cancer diagnoses to population-based cancer registries.
Legal Framework
This publication is important because registries are fundamental to surveillance, planning, evaluation, and research. Without a strong legal framework, cancer registration can remain incomplete or inconsistent.
The Toolkit
The toolkit combines a report with online tools to support legislation drafting while allowing adaptation to local contexts. It is relevant for health authorities and registry leaders seeking practical guidance.
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Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or European Health and Digital Executive Agency (HADEA). Neither the European Union nor HADEA can be held responsible for them.
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This project has received funding from the European Union’s EU4HEALTH Programme under the Grant Agreement no 101162959