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Clinical & Trials
Clinical evidence, investigations, and human-factors studies.
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All Clinical & Trials terms
- Adaptive Trial Design
- Adverse Event(AE)
- ALCOA+
- Analytical Sensitivity
- Bayesian Trial Design
- Blinding and Masking
- Case Report Form(CRF)
- Clinical Evaluation Plan(CEP)
- Clinical Evaluation Report(CER)
- Clinical Investigation Plan(CIP)
- Composite Endpoint
- Data Safety Monitoring Board(DSMB)
- Decentralized Clinical Trial(DCT)
- Early Feasibility Study(EFS)
- Electronic Data Capture(EDC)
- Feasibility Study
- First-in-Human Study(FIH)
- Human Factors Engineering(HFE)
- ICH E6 Good Clinical Practice(GCP)
- IDE Annual Progress Report
- IDE Supplement
- Informed Consent
- Institutional Review Board(IRB)
- Intent-to-Treat vs Per-Protocol(ITT / PP)
- Investigational Device Exemption(IDE)
- Investigator Brochure(IB)
- Investigator-Initiated Trial(IIT)
- Limit of Detection / Limit of Quantitation(LoD / LoQ)
- Lost to Follow-up
- Master Protocol (Basket / Umbrella / Platform)
- Minimal Clinically Important Difference(MCID)
- Non-Inferiority Trial
- Performance Study (IVDR)
- Pivotal Trial
- Pragmatic Trial
- Primary and Secondary Endpoints
- Propensity Score Methods
- Protocol Deviation
- Real-World Data(RWD)
- Real-World Evidence(RWE)
- Risk-Based Monitoring(RBM)
- Sample Size and Statistical Power
- Serious Adverse Event(SAE)
- Sham Control
- Source Data Verification(SDV)
- Surrogate Endpoint
- Trial Master File(TMF)
- Unanticipated Adverse Device Effect(UADE)
- Use Error