Event
2nd Annual Medical Device Safety And Regulations Compliance Forum
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June 1 - 2, 2023

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9:00am - 6:00pm

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Steigenberger Airport Hotel Berlin, Schönefeld, Germany

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The 2nd Annual Medical Device Safety And Regulations Compliance Forum will highlight the importance of driving technology and innovation across the industry supply chain, highlight the challenges faced due to changing regulations, consider what is needed to be compliant and secure certification for new products and how to ensure patients have access to the necessary medical devices. The Quality and Detect team will be exhibiting and Michael King will deliver the keynote presentation, “Designing A Global Health Hazard Evaluation & Recall/ Field Action Process(Es) That Meets Specific Requirements Beyond The EU/ US.”
Key Speaker

Michael King

Senior Director, Product & Strategy, IQVIA
As Senior Director of Product and Strategy within the Technology Solutions business of IQVIA, Michael King is responsible for ensuring that the Medical Device solutions have the necessary functionality to support the increasingly complex and diverse global regulations. He is particularly focused on optimising business workflows through intelligence driven simplification and automation within and across the Safety, Regulatory and Quality functions. Michael has over 15 years of knowledge and experience leading localised and global teams in Regulatory Affairs and Quality Assurance and has worked within the Medical and Surgical, Orthopaedic, In Vitro Diagnostic, Diagnostic Imaging, Dental and Urology sectors. Before joining IQVIA Michael was the Vice President of International Regulatory Affairs for a Dental Technology organisation and had oversight of the International Product Registration, Adverse Event Reporting and country-based Quality Management Systems. Michael holds a degree in Physics from Oxford University and briefly worked for a consulting firm in the telecommunications industry prior to beginning his career in the Medical Industry.
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