Journal article
SATURN: assessing the feasibility of utilising existing registries for real-world evidence data collection to meet patients, regulatory, health technology assessment and payer requirements
- Abstract:
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Background: SATURN (Systematic Accumulation of Treatment practices and Utilisation, Real world evidence, and Natural history data) for the rare condition osteogenesis imperfecta (OI) has the objective to create a common core dataset by utilising existing, well-established data sources to meet the needs of the various stakeholders (physicians, registry/dataset owners, patients and patient associations, OI community leaders, European [EU] policymakers, regulators, health technology assessments ...
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- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 1.1MB, Terms of use)
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- Publisher copy:
- 10.1186/s13023-024-03341-4
Authors
- Publisher:
- BioMed Central
- Journal:
- Orphanet Journal of Rare Diseases More from this journal
- Volume:
- 19
- Issue:
- 1
- Article number:
- 336
- Publication date:
- 2024-09-12
- Acceptance date:
- 2024-08-21
- DOI:
- EISSN:
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1750-1172
- Language:
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English
- Keywords:
- Pubs id:
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2027614
- Local pid:
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pubs:2027614
- Source identifiers:
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2256886
- Deposit date:
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2024-09-12
- ARK identifier:
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- Copyright date:
- 2024
- Licence:
- CC Attribution (CC BY)
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