Tailored to your device
Start with recommendations relevant to your device and the purpose of your review.
Plan, search, screen, appraise, extract and synthesise in one place. AI assistants propose at every step. Your reviewers confirm, edit or discard each proposal.
See the platform in actionScreening chart
Step 1
Get recommendations on sources, objectives and criteria, grounded in regulatory guidance. Create your review plan in one click.
Start with recommendations relevant to your device and the purpose of your review.
Define what the review needs to answer and how your team will assess the evidence. Get guidance on writing clear objectives and criteria that reviewers can apply consistently.
Confirm the plan and record your evaluators before screening begins, so your team works against the same criteria.
Step 2
Combine literature, post-market data and regulatory sources, with a clear record of where your evidence came from.
Bring in results from PubMed, Cochrane, Europe PMC, PMC, OpenAlex, Google Scholar, medRxiv, bioRxiv, PROSPERO, ClinicalTrials.gov and ICTRP. Use the browser extension, import PDFs directly or upload reference files from other databases.
Search incident reports, safety notices and recalls alongside health technology assessments, clinical guidelines, standards and regulatory guidance.
Get each source’s query proposed from your plan, translated for other databases and checked before you run it. Keep each search’s query, date and record count with your review, ready for the plan, the report and the PRISMA 2020 flow diagram.
Step 3
Screen against your agreed criteria, with a record of the decisions behind your evidence selection.
Bring results from different sources together. Resolve duplicates before screening, with possible matches flagged for review.
Get inclusion and exclusion proposals supported by reasons and quoted passages, at title and abstract and at full text. Your reviewers decide, with exclusions recorded against your criteria.
Use bulk actions, filters and highlighted passages to work through records efficiently. Track progress as your team screens.
Step 4
Assess study quality and collect the data your review needs, with the supporting passage always within reach.
Use established appraisal methods and levels of evidence, or apply your organisation’s own criteria consistently across studies.
Get proposed answers linked to the supporting passages. Your reviewers check and approve the extracted data.
Access available open-access PDFs or add full texts from your own collection. Read, highlight and capture relevant figures and tables alongside your review.
Step 5
Turn your reviewed evidence into the documents you need to hand over.
Bring findings together for each review question. AI proposes the synthesis, and your team reviews and edits it together.
Export your plan and report to Word or PDF, with a PRISMA 2020 flow diagram. Hand over screening results in Excel, the diagram as an image and references in RIS, BibTeX or EndNote.
Update your review without starting over. Keep continuity with earlier work and see what has changed.
Step 6
AI proposes. Your team decides, with a clear record of the work behind the review.
Every change is logged with who made it and when, for each review and across your organisation. Lock the review once it is approved.
Choose which AI assistants to use for each review. Your data is not used to train AI models.
Reviewers and collaborators work together, with access appropriate to their roles.
Give new team members a clear process to follow, with guidance at each step and the same review criteria as their experienced colleagues.