Post Market Surveillance.
Done For You.

Use our hands off process to complete your MDR PMS requirements.

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Vigilance

CiteMed Vigilance

What You Receive:

  • Quarterly Report PDF/Doc

  • Global Adverse Event Search

  • Key AE Reviewed + Highlighted

  • Tending Data + Benefit Risk Update
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Clinical

CiteMed Clinical

What You Receive:

  • Everything in CiteMed Vigilance

  • Comprehensive Global Lit Search Update
  • PMCF Full Document Draft
  • PDF/Word Versions of All Docs
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Success

CiteMed Complete

What You Receive:

  • CiteMed Clinical and Vigilance

  • PSUR Full Document Draft
  • Inclusion of your internal Data
  • Updated Benefit Risk
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WHAT IT’S LIKE TO WORK WITH CiteMed
Interview of Ed Drower (Director of Research at CiteMed) discussing Literature Search for MDR (also applicable to PMCF)
Our Comprehensive Search Capabilities

We take a global approach to our Literature Search and Evaluation. Our experts compile and review Adverse Events and CLinical Literature from a long list of sources. The result is an undoubtedly thorough submission to satisfy any Notified Body Assessor’s concerns.

Featured Post Market Surveillance Articles and White Papers
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Post Market Clinical Follow-Up (PMCF) – Understanding MDCG’s Latest Guidance
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Notified Body

Building Your PMS Templates
(WhitePaper)

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Clinical Evaluation Process
Post Market Clinical Follow-Up (PMCF) – Understanding MDCG’s Latest Guidance
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