Build a winning EU MDR strategy for your medical devices

Richard Jones
MDR Compliance Webinar - A masterclass on building a winning EU MDR strategy for your medical devices

Our CEO, Dr Paul Hercock, recently presented one of our free MDR Compliance Webinars - A masterclass on building a winning EU MDR strategy for your medical devices. You can watch it here:

Webinar goals

  1. Gain a detailed overview of the MDR
  2. Understand the key requirements for MDR compliance
  3. Confidently build active regulatory systems to MDR standard
  4. Turn regulatory obligations to your wider advantage
  5. Generate and interpret clinical evidence to support your MDR submissions
  6. Access powerful resources and personal support

Feedback

The webinar was well received and some of the comments from the participants included:

  • Thanks a lot guys. This was a clear overview and informative as well. YB

  • Thank you very much for the session. I will be in touch with you about your Academy. TC

  • Thank you very much for the step by step analysis on MDR compliance. SSY

  • Thank you so much. GM

We will be running more webinars throughout the year so please subscribe to our newsletter to be notified when we schedule our next one.

Back to top

Related articles

  1. A futuristic user interface is operated at a desk.

    An Overview of the UK’s 2024 Post-Market Surveillance Update

    What might mandatory PMS plans - which emphasise enhanced patient engagement and proactive risk management - mean for the industry?

    Ron Sangal Ron Sangal Lead Medical Writer
  2. MEDICA 2024

    Mantra Systems at MEDICA 2024

    Mantra Systems is going to MEDICA 2024, the largest medical trade fair in the world. We hope to see you there.

    Richard Jones Richard Jones Operations Director
  3. EU flags

    Regulation (EU) 2024/1860 - Its impact on EU MDR and IVDR

    How does the recent Regulation (EU) 2024/1860 amendment affect the EU MDR & IVDR?

    Shona Richardson Shona Richardson Regulatory Medical Writer
  4. EU flag

    MDCG 2024-10 - Orphan medical devices

    How to apply MDR pre-market clinical evidence requirements to medical devices intended for limited usage.

    Dr Simon Cumiskey Dr Simon Cumiskey Senior Lead Medical Writer
  5. MEDICA 2023

    Mantra Systems at MEDICA 2023

    Mantra Systems is going to MEDICA 2023, the largest medical trade fair in the world. We hope to see you there.

    Shen May Khoo Shen May Khoo Junior Regulatory Specialist
  6. Simplifying the challenges posed by the new EU MDR

    Simplifying the challenges posed by the new EU MDR

    Our CEO Dr Paul Hercock was invited to speak on a Kaizen Life Sciences podcast about the challenges posed by the EU MDR.

    Dr Victoria Cartwright Dr Victoria Cartwright Relationship Manager
  7. EU flag

    A proposal to delay the EU MDR gets approved

    A vote in the European Parliament has decisively approved a delay to full implementation of the EU MDR by one year.

    Richard Jones Richard Jones Operations Director
  8. EU regulators may delay MDR enforcement

    EU regulators may delay MDR enforcement. Out of the woods?

    A delay of the MDR would be welcome news for many, but what would a delay mean in practice? To what extent can preparations for EU MDR be put on ice?

    Dr Paul Hercock Dr Paul Hercock Chief Executive Officer

More articles

Do you need support with your medical device approval strategy?

Contact us today