Sammanfattning
Data from several different monitoring systems are examined. The potential for registers based on data obtained from clinical practice, and linkage of such data to national health and population registers, is discussed. The approach described is a possible prototype for long term surveillance systems needed for the safe introduction of new treatments.
Originalspråk | engelska |
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Sidor (från-till) | 707-712 |
Tidskrift | Annals of the Rheumatic Diseases |
Volym | 65 |
Nummer | 6 |
DOI | |
Status | Published - 2006 |
Ämnesklassifikation (UKÄ)
- Reumatologi och inflammation