Frame the question
Define the population, device or intervention, comparator, outcomes, study designs, and intended regulatory use.
Book a Scoping Call Clinical Evidence Synthesis
Systematic literature reviews for medical devices using documented search, screening, appraisal, extraction, and evidence synthesis methods.
The IMTS perspective
Medical device literature reviews support clinical evaluation, regulatory submissions, state of the art assessment, safety surveillance, PMCF, and scientific publication. IMTS designs reproducible searches and converts complex evidence into structured conclusions that answer the intended regulatory or scientific question.
The usefulness of a review depends on decisions made before the first search is run. The question, eligibility criteria, databases, appraisal method, extraction fields, and synthesis plan must be aligned with the document the evidence will support.
Scope of support
How we work
Define the population, device or intervention, comparator, outcomes, study designs, and intended regulatory use.
Document searches, screening decisions, appraisal, and extraction using consistent methods and quality controls.
Explain patterns, limitations, gaps, and applicability so the evidence directly supports the target document.
Start a conversation
We will help define the scope, source materials, review process, and practical next step.
Book a Scoping Call