A Literature Review Process That Fits Your Team
Which Literature Review Do You Need?
Full Systematic Literature Review
Our Literature Reviews are designed to be used in EU MDR CERs, or IVDR PERs.
CAPA/Audit Lit Review
Our light speed timelines make our Lit Reivews ideal for sorting out CAPAs during an Audit.
Do It Yourself Review
If you want to conduct your own, use our battle tested Template, and our Software tool to save 10x the hours on your review.
Do It Yourself Review
If you want to conduct your own, use our battle tested Template, and our Software tool to save 10x the hours on your review.
Literature Review and Updates: When You Need Them
Imagine having a system and process in place to conduct your searches, store your evaluations, and track updates with ease year after year. For all of your devices. Too good to be true? We don’t think so.
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If you already know what you’re doing and just need a system, use our platform. If you are short on time, our team of Notified Body approved Medical Writers are just one click away to take the reigns and complete full Literature Reviews for your submissions.
Notifed Body Approved Writers
Our writers have the chops to tackle any classification of device for MDR, and the CVs to submit alongside your final document. Our team has cumulatively written well into the 100s of CERs on all device classifications.
Consistent Updates
Keep your Literature Review, and CER documents updated year after year without worry or hassle. We keep everything organized and audit ready.
Post Market and Vigilance Data Support
Did we mention our Literature Reviews include Adverse Event and Vigilance Data?
If you have a team and process in place for PMS, great! If you don’t, our comprehensive PMS packages are easily integrated into your CER. All of it meticulously tracked and stored on our platform for you.
FEATURED IN
Are You Ready to Work With Us?
If You Are:
What’s included in a CiteMed Literature Review?
Systematic Literature Review
Bring your own, use our software system, or let our experts conduct a bullet-proof SLR for your CER
EU MDR Template and Strategy
We focus exclusively on EU MDR, so you can be assured our template is audit-tested and ready.
Qualified Review
Worried your CV won’t be enough for your auditor? Our writers are all Notified Body approved for submission.
PMS Planning and Reporting
We advise, draft, and execute plans for PMS compliance on all device classifications. Have your own already? No problem.