ENCePP Code of conduct

No
Data sources

Data source(s), other

National MS registry ReMuS Czechia

Data sources (types)

Other

Data sources (types), other

The aim of the study is to characterise the safety profile of natalizumab in a routine clinical practice in the Czech Republic by monitoring serious adverse events (SAEs).
Use of a Common Data Model (CDM)

CDM mapping

No
Data quality specifications

Check conformance

Unknown

Check completeness

Unknown

Check stability

Unknown

Check logical consistency

Unknown
Data characterisation

Data characterisation conducted

No