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Better Systematic – Literature Reviews 5 . Times. Faster.

(With No Set-Up or On-boarding Pains).
Software built by seasoned Medical Writers. Save absurd amounts of time on labor intensive literature review so you can spend it on Regulatory work that matters.

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WHAT WE ARE

What if you could increase the productivity of your clinical literature team, standardize all your systematic reviews, reduce costs, and keep your devices/drug literature up to date year after year (without massive shared spreadsheets and folders, and lost information due to staff turnover)?

Delightfully efficient
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Delightfully Efficient

A meticulously refined research software tools platform, designed to speed up your evidence based practice Literature Reviews, and make long-term organization and maintenance of your Clinical Literature simple and streamlined. You provide the expertise, we provide the efficiency.

Delightfully efficient
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Works Out of The Box

A completely functional ‘out of the box’ systematic review process crafted by seasoned Regulatory Affairs over hundreds of cumulative systematic reviews and submissions.

Delightfully efficient
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Robust and Customize-able

Fully customizable to your preferred search strategy.

We Are Not:

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A fully automated, black box ‘AI’ system that promises to perform your reviews at the click of a button.

Customizable literature review
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A general ‘catch all’ systematic review tool that takes weeks of configuration and training to use properly.

Customizable literature review

From Zero to Running Your First Systematic Review in Minutes

We hate long, expensive on-boarding processes.

That’s why we’ve spent countless hours re-working our software to be as straightforward from initial login to conducting systematic reviews.

A Compliant and Documented Review. Every Time

Abstract Review

You now have a duplicate-free, color-coded list of abstracts to review. Happy clicking!

Detailed Review

On Your Included Articles, Upload the Full Text PDFs, and get to reading! For each article you can extract out the data your want (safety, performance etc.) in a fully customizable form.

Generate Final Systematic Review Report

Generate your full Systematic Literature Review report. Have a large team, and need a more complex process? No problem either, work with our dedicated RA and software experts to craft your ideal workflow.

Compliant and Documented Review
Compliant and Documented Review
  • Medical Device Regulatory Submissions
  • Clinical Evaluation Report Supporting Literature Review
  • Vigilance Reporting and Review
  • Pharmaceutical Post Market Surveillance
  • Product Development Research
  • Competitor Research and Analysis
  • Duplications Marked and Removed Automatically
  • GRADE Analysis
  • PICO Keyword Highlighting
  • Customizable Extraction Fields
  • Medical Device Adverse Event Searches
  • Outputs Generated in Word, and MS Excel — Direct Input into CER
  • Import and integrate from OneNote and various tools.

MDR Compliance — Our team uses this exact process and system to produce a LOT of MDR compliant literature reviews. We’ve had 100% success with our literature reviews on submission.

Compliant and Documented Review
Manage Updates With Ease

Manage Updates With Ease

Keep your literature reviews organized and updated with an easy-to-manage workflow.

Built For Regulatory and Clinical Professionals

Our Regulatory experts use this platform daily, and are constantly tweaking and refining it towards a perfect review.

Leading De-Duplication

Save hours sorting through Citations with our de-duplication methodology. Works across ALL databases and citations.

Global Searches

We support all major databases (PubMed, PMC, Embase, Cochrane, ClinicalTrials.gov) and more!

Customizable Extraction Fields

Use our European/American compliant fields or customize your review.

Adverse Event and Vigilance Searching

Search, Sort, Review, and Process all Adverse Events on your Device or Drug.

Privacy and Security

Have full transparency and peace of mind on when and how your business data is being used.

Word, Excel, EndNote Integrations

Generate a ready-to-submit Word Document, or Export to Endnote and Excel.

Transparent Pricing

Transparent Pricing

Pay for what
you’re using.

No ballooning costs per seat like other subscription based tools, or locked away features.

Bullet-Proof Validation Process

Leave your auditor speechless, with our detailed protocols generated based on your search, and documented systematic review validation process.

All search results are documented, timestamped, and neatly packaged for your regulatory submission needs.

All references are documented in the final outputs, and displayed in an easily readable layout.

Bullet-Proof Validation Process

Frequently Asked Questions:

There are plenty of good tools out there. The CiteMed SLR tool stands out in that it’s been built and designed specifically to help on medical device regulatory submissions. You can get set up, and have a fully compliant search protocol generated before your morning coffee gets cold. We’re that streamlined. We can talk all day about our features, but the reality is that they’re better shown in a free demo.

We pull automatically from PubMed, PubMed Central, Cochrane Library, Clinical Trials.gov and FDA Maude. But we support even more, including EMBASE if you upload your search results file. If we don’t have it, we’ll build it for you!

Yes, we can take your citations from an Endnote file and import them into the system. Going the other way, we can export into a format that will make ‘Cite While You Write’ work easily with Endnote and Word.

Polished Product – You will see a final, fully formatted product customized with your branding Revisions – Our staff is prepared to complete revision requests in the same business-day

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