Our role is to collect and protect
skin registries and their communities
Our objectives:
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Information Networking
Building connections between clinical data, collaborative partners, patient organisations and our registries
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Knowledge
& Insight
Provide consultation on the development and governance of dermatology registries
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Improving Research
Collecting the data of consenting patients to generate anonymised data points for research to improve their lives
![](https://nisrsolutions.com/wp-content/uploads/2021/04/home-icon-04.png)
Data
Analyses
Statistical analyses of anonymised registry data and support with data interpretation and publication
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Protecting Data
Standardized oversight of registries and stewardship of data to GDPR data protection standards