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For Perfectionist Medical Writers On A Deadline
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We all know Systematic literature review is an essential part of any regulatory process. We also know it’s a complete labor-intensive pain to perform and maintain without making mistakes.
That’s why we built CiteMed, to keep our own medtech writing team from setting fire to their laptops trying to keep up with generating error-free SLRs day in and day out.
We didn’t have time to onboard or learn (or pay for) some absurdly complex enterprise package of software, so we built something simple. Our users can:
CiteMed.io was designed for you and your team to sit down and start reviewing. That’s it. You’re not going to find 3 weeks worth of training videos, multi-hour ‘strategy-calls’, or powerpoint presentations made by consultants who have never written so much as a postcard.
We know our workflows are great, because we’ve used them to successfully submit 100s of our own reviews and documents (see our track record at Cite Medical!). So we suggest you give us a shot and see if our tool can work for you too. Free evaluation periods are always available to try it out.
P.S. If you’re a big team with a complex workflow, we’re not opposed to building you something special to suit your needs… but it won’t be today. CiteMed.io as it’s currently designed is for reviewers that are ready to get traction immediately.
We built CiteMed to solve our own problem, which was juggling a mountain of Systematic Literature Reviews for our medical device clients. It’s been forged through our mistakes, aspirations, and ideas over the course of 7 years and we don’t intend on stopping or selling out.
Whether you’re a department of one, or managing a team of 50 writers we’re set up to get you results without the fuss of enterprise level configuration and training. If you’re committed to performing the highest caliber of literature review (in any industry), we’ve got you covered.
For freelancers and small teams:
For Enterprise and Big Teams:
We don’t want to just send you a login and say ‘Ciao Ciao’, our experienced writing team (hundreds of successful submissions) continues to put together best-in-class instructionals on the latest Regs in EU and US, and a strong focus on evidence and literature review.
Better evidence means safer products, and healthier outcomes. Join us in the never-ending quest to process and evaluate evidence.
