Medical-research lens · The CASRAI biomedical hub
Medical research
Medical research has the densest research-administration overlay of any field: ICMJE authorship, CRediT contributions, ICH GCP, IRB / REC, CONSORT / STROBE / PRISMA, clinical-trial registration, FDA / EMA / MHRA filings, AI-model disclosure for clinical AI, FAIR-data deposit for trial datasets, and increasingly tight conflict-of-interest disclosure. This hub knits the relevant CASRAI guidance into a single coherent path.
What sits inside the medical-research lens
Four-layer stack: (1) authorship + contributorship — ICMJE + CRediT used together; (2) reporting standards by study type — CONSORT for RCTs, STROBE for observational, PRISMA for systematic reviews, ARRIVE for animal studies, SPIRIT for trial protocols; (3) regulated submissions — FDA, EMA, MHRA, PMDA; (4) responsible AI and data — FDA AI/ML Action Plan, EU AI Act for clinical AI, FAIR-data deposit via clinical-trial registries + clinical-data repositories.
Specialty pages
Pick your area
Specialty
Oncology
Cancer research — RECIST, CONSORT-extensions, NCI Common Data Elements, ImmunoSig.
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Clinical trials
ICMJE + CONSORT + SPIRIT + ICH GCP — the four-letter trial-conduct alphabet.
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Infectious disease
Outbreak response publishing, ISARIC tier-1 data, WHO R&D Blueprint, MIRDD-style metadata.
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Neuroscience
NIH BRAIN initiative, NWB (Neurodata Without Borders), FAIR neuroimaging (BIDS), CRediT for compute-heavy labs.
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