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Speaking Engagements

  

It’s no secret that the future of the Healthcare Industry lies in technology. Medical Devices have the potential to revolutionise medical treatments, diagnostics, patient engagement and quality of life. Yet, innovation comes with ever increasing regulatory scrutiny and security challenges.

22-24 February 2022
  

MD&M West brings together medtech engineers, business leaders, disruptive companies, and innovative thinkers to create powerful solutions and life-changing medical devices.

12-14 April 2022
  

Bringing Competent Authority, Notified Body and industry experts together to discuss the evolving global regulatory landscape 9 focused tracks: EU MDR. IVD Regulation and Strategy. Software and AI. Legal and Compliance. Post Market Surveillance & Vigilance. Clinical Evaluations & Investigations. Global Market Regulations. Biocompatibility.

20-24 June 2022
  

It’s no secret that the future of the Healthcare Industry lies in technology. Medical Devices have the potential to revolutionise medical treatments, diagnostics, patient engagement and quality of life. Yet, innovation comes with ever increasing regulatory scrutiny and security challenges.

13-15 September 2022
  

MEDICAL DEVICE REGULATIONS ACROSS THE GLOBE: YOUR DEDICATED HUB TO ACHIEVING COMPLIANCE Combining FDA, Notified Body and Industry Perspectives to Shape the Future of Medical Device Regulations 4 Tracks across 3 days: Medical device regulation and implementation. Biocompatibility. Software and AI for Medical Devices. In Vitro Diagnostic Regulations.

06-08 December 2022
  

Now in its 3rd year, this ambitious event unites software engineering, quality assurance and regulatory experts as well as regulatory bodies such as the GMED and hospital representatives to cover medical device software development challenges in a “lifecycle” manner sequentially covering agile development, usability, compliance, cybersecurity, risk