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Access limitless support from our Regulatory Experts!
No one wants to pay giant monthly fees for software when they don’t have any relevant projects to work on.
Have a few team members you want to help you with reviews? No problem, we don’t charge for additional users on our Freelancer Tiers.
We’ve got you!
Want to focus on other parts of your contract and save yourself some time?
We can do full literature reviews end-to-end (performed by a qualified medical writer for any kind of Regulatory submission).
We know this works, because we use it ourselves every single day.
If our platform doesn’t save you time, we’ll give you your money back.
Simple as that.
Have a question that you can’t find the answer to? Drop us a line and we’ll try and answer it the same day.
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.
We output to Excel, Microsoft Word (Submission ready documents), in multiple displays of your review results. Your full review, list of citations, search files for validation… we accommodate it all.