Clinical evaluation for Class III devices — do you have what it takes?

Live seminar 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. An in-depth exploration of preparing towards and conducting clinical evaluation of Class III medical devices.
  2. Understand the impact of this risk classification on designing and implementing clinical evaluation activities.


  • Live seminar: Clinical evaluation for Class III devices — do you have what it takes?
  • Date: 30th September 2020
  • Time: 10am
  • Duration: 6 hours
  • Location: Fusion at Magna Business Centre, Rotherham
  • Delegate fee: £650 (includes lunch & refreshments)

Register your place

Due to the current coronavirus pandemic, our live seminars are set with provisional dates. Registration is open, but we are guided by advice from the UK Government. When restrictions are lifted enough for us to run them safely, we will email each delegate and ask them to confirm their place.

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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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

    • Designing your PMS system
    • Vigilance systems
    • Medical complaints
    • Writing PMS plans & PSURs
    • Clinical investigations & product registries
    • Risk management
    • Identify needs for any PACAs / FSCAs
  • 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

    • Design your PMCF strategy
    • Build Medical Device Product Registries
    • Ensure complete lifecycle evidence generation
    • Prepare evidence reports for other departments
    • Reduce time waste on administration
  • 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

    • Performing 360-degree Clinical Evaluations
    • Write & review CERs
    • Systematic literature appraisals
    • Clinical evidence Gap Analyses
    • Clinical development plans
    • Designing & implementing clinical investigations
  • 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

    • Identify your product's general SPRs
    • Find gaps in existing evidence portfolio
    • Systematic literature reviews
    • Clinical development plans
    • Impact analysis on Risk Management processes

Do you have any questions about our services or training?

Contact us