MDR Compliance for Class I devices

Online workshop overview

  • In-depth training on a range of highly-targeted topics to ensure you get exactly what you need for your MDR transition.
  • Delivered in-person by our medical experts, live seminars offer a unique opportunity for tailored hands-on training.
  • Ongoing access to our Q&A follow-up system following seminar completion.


  1. Understand the specific requirements for MDR compliance of Class I medical devices.
  2. Understand how requirements differ from those under MDD.
  3. Learn what to do to prepare your regulatory strategy for full implementation of the MDR.


  • Online workshop: MDR Compliance for Class I devices
  • Date: 16th September 2020
  • Time: 12 noon
  • Duration: 2 hours
  • Location: Online
  • Delegate fee: £350

Register your place

After registration, we will send you a confirmation email with further instructions.

This is not a committment to buy. We will contact you in due course to confirm your place. If you subscribe to our newsletter, we will send you periodic email updates. You can unsubscribe at any time. Your privacy is important. See how we handle your data.


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Any questions?

If you have any questions about our MDR training, please get in touch.

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Download our free Mastering the MDR White Paper — Our easily digestible summary of the EU MDR


MDR Services

Our team of medical doctors are specialists at building the clinical evidence portfolio that you need for MDR compliance of your products.

  • Through our bespoke Post-Market Surveillance (PMS) service we will apply clinical knowledge to design, update, implement, and maintain your MDR compliant PMS systems.

    Learn more about our Post-Market Surveillance service

    • PMS system design
    • Vigilance systems
    • Complaints handling
    • PMS plan & PSUR writing
    • Clinical investigations
    • Risk management
    • PACA / FSCA need identification
  • Our medical experts will design a robust and adaptable clinical evidence generation system to collect Post-Market Clinical Follow-up (PMCF) data on your medical devices.

    Learn more about our Post-Market Clinical Follow-up service

    • PMCF strategy design
    • Build Medical Device Registries
    • Complete lifecycle evidence generation
    • Evidence reports for other departments
    • Reduce administration time
  • Our full Clinical Evaluation service involves a 360-degree analysis of your medical devices, writing and reviewing CERs, and designing clinical development plans.

    Learn more about our Clinical Evaluation service

    • 360-degree Clinical Evaluations
    • CER writing / reviewing
    • Literature appraisals
    • Clinical evidence Gap Analysis
    • Clinical development plans
    • Clinical investigation design / implementation
  • Our medics will apply powerful clinical techniques to quickly and effectively identify and minimise any gaps in your clinical evidence portfolio.

    Learn more about our Gap Analysis service

    • Genreal SPR identification
    • Evidence portfolio gap analysis
    • Literature reviews
    • Clinical development plans
    • Risk Management impact analysis

Do you have any questions about our services or training?

Contact us