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To better assist you with your request, please choose a research area provided by The University of Sheffield, ScHARR. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.

Clinical Trial Design

Develop study-related protocols, case report forms (CRFs) and database tools for records management.
Health Economics and Outcomes Research (HEOR)

Evaluate data collected during drug development to maximize the value of a therapeutic product.
Discovery Statistical and Mathematical Modeling

Use mathematical variables and equations to establish relationships between data.
Systematic Literature Review

Summarizes the results of research (that meet pre-defined eligibility criteria for inclusion) and provides a high level of evidence on the outcomes assessed.
Patient Reported Outcomes (PRO)

Assessment of health outcomes directly reported by the patient who experienced it, without interpretation of the patient's response by a clinician.
Health Technology Assessment Submission (HTA Submission)

Analyze the medical, social, ethical, humanistic, and economic considerations of a drug, medical device, or clinical procedures. Submissions are sent to regulatory agencies with different requirements that govern submissions. See also AMCP and Value Dossier.
Bayesian Statistics

Extract information from data sets that are subject to error or noise to see unobserved possibilities.
Viral Infection Models

Measure therapeutic endpoints in animal models of viral infection.
Clinical Trial Reporting

Report results of clinical trials to regulatory agencies. This includes participant flow, baseline characteristics, outcome measures, statistical analyses, and adverse events.