Literature search review, reimagined
From PICO query to data extraction — DocliMed gives clinical research teams one focused workspace for every stage of systematic review.
Built for
Live workspace
Review Pipeline
12 MeSH terms, 3 synonym rows, Title/Abstract + MeSH fields
142 of 238 articles reviewed by 2 independent reviewers
Awaiting included studies from screening stage
238
Articles
4
Reviewers
67
Included
5
Literature databases
7
Vigilance sources
2
Independent reviewers per study
DOCX
Regulatory-ready reports
Why DocliMed
How DocliMed will help you
DocliMed leverages cutting-edge AI to seamlessly automate clinical, regulatory, and quality operations — so your team can focus on what matters most.
Built for MedTech & Pharma compliance
Comprehensive Device Support
Effortlessly handle your entire product portfolio, regardless of device risk classification.
Unlimited Portfolio Growth
Designed for any scale — whether you are an emerging SME or a multinational enterprise managing thousands of Technical Files.
Audit-Ready Global Compliance
Navigate complex international landscapes with built-in compliance for EU MDR, IVDR, FDA and global standards.
Fast
Accelerate every stage of your workflow with DocliMed's technology. Automate repetitive steps, connect your data points and sources, and retrieve research instantly — so your team spends less time searching and more time deciding.
Adjustable
Shape your review and appraisal workflows to match the way your organization actually works. From process design to how outcomes are exported and reported, DocliMed adapts to your requirements — not the other way around.
Easy to Use
Customers consistently rate DocliMed as intuitive and easy to adopt. With multiple integrated solutions on a single platform, your team gains not just usability, but multiplied productivity.
Collaborative
Bring your team's knowledge together. Collaborate in real time, assign tasks and deadlines, and give colleagues the visibility they need — building a more transparent, connected way of working.
Scalable
From a handful of users to organizations managing hundreds of users and thousands of articles, DocliMed scales with you — without compromising performance or reliability.
Compliant
Built on a secure foundation aligned with ISO 27001 practices, full alignment with privacy and GDPR requirements, and complete traceability. Every action is audit-ready, so compliance is never an afterthought.
How it works
Four steps from research question to evidence synthesis
Each stage hands off cleanly to the next. Your team always knows what comes after search, screening, or extraction.
Build PICO Query
Define population, intervention, comparison, and outcome with MeSH terms, synonyms, and Boolean logic.
Multi-Database Search
Search across PubMed, Europe PMC, Cochrane, and Google Scholar — millions of biomedical articles from one interface.
Screen Articles
Review abstracts with include/exclude decisions, track inter-reviewer agreement, and resolve conflicts.
Extract Data
Capture study design, outcomes, risk of bias, and quality notes in structured, repeatable fields.
Platform
Everything your review team needs
Purpose-built tools for each stage of systematic review, designed to reduce friction and keep your evidence pipeline moving.
PICO Search Builder
Build structured queries with MeSH terms, synonyms, and per-row field tags. Preview the full PubMed query before executing.
Evidence Screening
Include or exclude articles with a structured review flow. Track reviewer progress and maintain complete audit trails.
Data Extraction
Capture study design, primary outcomes, risk of bias, and quality notes in a consistent, structured format.
Team Collaboration
Shared workspaces with role-based access, invitation flows, and visibility into team progress across every stage.
DocliMed Search
Search the MedTech and Pharma Landscape with DocliMed
Access the latest updates and news from regulatory authorities and industry, alongside databases, websites, profiles, document guidelines, images, and more — all in one place.
DocliMed Search draws exclusively on trusted sources, making it a reliable, structured information portal. Purpose-built with advanced search features and using AI, it helps you find accurate, relevant information in seconds.
Our mission is to empower professionals with instant access to medical industry information — combining publicly available, trusted websites, pages, and databases with DocliMed's own curated resources and data, maintained by our dedicated research team.
DocliMed Search
Profiles, databases, resources
Profiles
Core records
- Countries & authorities
- Manufacturers
- Hospitals
Product databases
By product type
- Medical devices
- In vitro diagnostics
- Software & apps
- Pharma
Resources
Clinical knowledge
- Treatments & conditions
- State of the art
All the MedTech and Pharma Intelligence You Need
Powerful Search, Real-time Updates and Fully Organized
Fundamentally, DocliMed is a data platform — powered by advanced software products and solutions built to make sense of complexity.
Every day, DocliMed collects and organizes vast amounts of information, much of it highly complex in format and structure. Behind the scenes, data science (coding, mathematical models and AI), work with algorithmic precision to transform raw data into information at your fingertips.
The result: powerful automation combined with complete flexibility. Customize your workflows, shape your data, and perform your tasks without restrictions — just you, the data, and the insights you need.
Regulatory and Clinical Strategy
Five principles that shape every pathway
How regulatory and clinical pathways are planned, submitted, and maintained across the product lifecycle.
Strategic
Regulatory pathways are aligned to business and clinical objectives from the outset — not bolted on after development decisions are made.
Precise
Submissions are built on data-driven evidence and exact documentation, leaving no ambiguity for reviewers to resolve.
Compliant
Every action is measured against current global standards, keeping the dossier defensible during audits and inspections.
Agile
The strategy adapts quickly as regulations, guidance, and market requirements shift, without losing course.
Transparent
Communication with Notified Bodies and Health Authorities is clear, timely, and fully documented at every stage of review.
These principles guide our Strategic Consulting and Medical Writing services — audit-ready documentation for MDR, IVDR, and FDA submissions.
Explore servicesFAQ
Common questions from research teams
Can't find what you're looking for? Reach out to our support team.
DocliMed is designed for medical research teams, systematic reviewers, clinical evidence groups, and health technology assessment organizations that need a structured, collaborative literature review workflow.
The builder lets you define structured search components (Population, Intervention, Comparison, Outcome) with support for MeSH terms, synonyms, per-row field tags (Title/Abstract, MeSH Terms, All Fields, etc.), and Boolean operators. It generates a valid PubMed query string you can preview and refine.
Yes. Projects support shared workspaces with invitation flows and role-based access. Team members screen articles independently, and the platform tracks progress and flags conflicts for resolution.
DocliMed searches across PubMed, Europe PMC, Cochrane Library, and Google Scholar — giving you access to millions of biomedical articles from a single interface.
Yes. DocliMed supports Clinical Evaluation (MDR) and Clinical Performance (IVDR) work — including systematic literature search across major scientific and vigilance databases with transparent methodologies and robust appraisal according to MDR Annex XIV, IVDR requirements, MDCGs and MEDDEV guidance.
Yes. Our specialized medical writing team helps medical device and IVD manufacturers create clear, audit-ready technical and clinical documentation for MDR, IVDR, and FDA submissions — from development phase through post-market lifecycle management.
All data is encrypted in transit and at rest. Projects are isolated by workspace, and access is controlled through role-based permissions with full audit logging.