Medical device evidence synthesis, delivered faster
Synthesa helps medical device companies identify, evaluate, and synthesise evidence to support medical strategy, market access discussions, reimbursement planning, and evidence-based differentiation.
1,000,000+
abstracts screened
20,000+
outcomes meta-analysed
7 to 14 days
average project delivery
When the evidence exists, but it is scattered across years of literature
Medical device evidence is often fragmented. Relevant studies may span different device generations, procedures, patient groups, clinical endpoints, and comparator approaches. Some evidence may be directly about your device, while other evidence may relate to a broader device category or procedure.
This makes it difficult for teams to answer practical questions quickly:
- What does the literature actually show?
- Which outcomes are most consistently reported?
- Where is the evidence strong, limited, or conflicting?
- Can existing evidence support a strategic or commercial claim?
- Is a new study needed, or can published evidence answer the question?
Synthesa helps medical device teams move from scattered literature to structured evidence quickly, using AI-powered workflows reviewed by evidence synthesis experts.
Evidence synthesis for device strategy, value, and communication
Clarify the evidence behind your device or device category
Synthesa helps teams identify whether the published literature supports meaningful differentiation around outcomes, patient populations, procedures, or comparators.
Useful when you need to:
- Understand whether evidence supports a device advantage
- Compare outcomes across studies or device categories
- Identify favourable and unfavourable evidence
- Build a structured evidence base for scientific communication
- Support medical, commercial, or partner discussions
Relevant services
Systematic Reviews, Meta-Analysis, Rapid Evidence Synthesis
Organise evidence for payer and market access discussions
Medical device market access often depends on a clear understanding of clinical value, outcome improvements, patient relevance, and comparative evidence.
Synthesa helps identify and synthesise relevant evidence to support these discussions.
Useful when you need to:
- Understand the published evidence around clinical value
- Summarise outcomes relevant to payer or reimbursement conversations
- Identify evidence gaps before deeper evidence generation
- Compare outcome evidence across device categories or procedures
Relevant services
Systematic Reviews, Meta-Analysis, Network Meta-Analysis
Know where the literature is strong, weak, or incomplete
Before investing in new studies, device teams need to know what the existing evidence can already answer.
Synthesa can map the available literature, identify gaps, and show where further research may be needed.
Useful when you need to:
- Decide whether additional studies are necessary
- Identify under-researched outcomes or populations
- Understand how much evidence exists in a device category
- Prioritise future evidence generation activities
Relevant services
Rapid Evidence Synthesis, Systematic Reviews, Abstract Screening
Use existing evidence before committing to expensive new research
In some cases, published evidence may already contain the answer a team needs. Synthesa helps evaluate whether existing literature can support decision-making before committing to a larger, self-funded clinical study.
Useful when you need to:
- Explore whether published evidence can answer a strategic question
- Assess feasibility before funding new research
- Build a preliminary evidence base quickly
- Understand whether a full systematic review or meta-analysis is justified
Relevant services
Rapid Evidence Synthesis, Systematic Reviews, Meta-Analysis
Clear evidence outputs for medical device teams
Depending on your project, Synthesa can deliver a focused evidence review or a full systematic review and meta-analysis.
Deliverables can include:
- Screened abstracts with inclusion and exclusion decisions
- Evidence maps by device category, population, comparator, or outcome
- Study characteristic tables
- Clinical outcome summaries
- Evidence gap assessments
- Data extraction tables
- Frequentist or Bayesian meta-analyses
- Network meta-analyses where relevant
- Publication-ready figures, tables, and summaries
- Structured reports for internal, medical, or commercial use
Medical device evidence synthesis delivered in 2 weeks instead of 3 months
Medical device evidence synthesis delivered in 2 weeks instead of 3 months
A medical affairs team at a medical device company needed to establish the evidence-based advantage of their type of device. Instead of initiating a new self-funded clinical study, the team wanted to understand whether existing published evidence could answer the question. The evidence was scattered across many years of literature, but the answer was available.
Synthesa completed:
- Literature screening
- Data extraction
- Outcome synthesis
- Full meta-analysis
The expected traditional timeline was 3 months. Synthesa delivered the project in 2 weeks.
A faster route from literature to evidence
Traditional CRO workflows can be valuable, but medical device teams often need a faster, more focused way to understand the evidence base.
Synthesa combines AI-powered workflows with evidence synthesis expertise to accelerate literature-heavy projects without requiring your team to adopt new software.
Traditional CRO workflow
- Longer setup and delivery timelines
- High manual screening burden
- Slower for exploratory or time-sensitive questions
- Less practical for very large literature sets
- Often requires larger project commitments
Synthesa workflow
- Average project delivery in 7 to 14 days
- Screening and extraction at AI scale
- Expert validation and quality control
- Suitable for fragmented and high-volume device literature
- Free abstract screening pilot available for qualified projects
AI-powered evidence synthesis, delivered as a service
Synthesa is not another software platform your team needs to learn.
You define the evidence question, criteria, and required outputs. We manage the AI-powered workflow, expert review, synthesis, and delivery.
Your team receives structured evidence without having to configure tools, train users, or build an internal AI review process.
- No new software to learn
- No internal AI workflow to manage
- Expert-reviewed outputs
- Transparent screening and synthesis logic
- Structured deliverables ready for team use
Start with a free abstract screening pilot
For qualified projects, Synthesa can screen a defined set of abstracts using your search strategy and PICO criteria.
The pilot can run in parallel with your current review process or be compared against a completed project.
What you receive
- Screened abstract list
- Inclusion and exclusion decisions
- Screening based on defined criteria
- Delivery within a few days
- A practical way to evaluate Synthesa before a larger project
Need to understand your medical device evidence base quickly?
Tell us about your device, evidence question, literature set, or timeline. We can help you decide whether to start with a free pilot, a rapid review, or a full systematic review and meta-analysis.