The Future of Quality, Regulatory and Safety in the MedTech Industry
How are evolving regulations affecting the MedTech landscape?
Regulations used to be seen as a barrier to business, now they’re increasingly recognized as an integral business function. Listen to top regulatory and quality experts discuss factors that are driving regulatory change in the MedTech industry and how companies can keep up with these changes to help access global markets.
‘The regulation of medical devices is inherently complicated.’
Phil Brown, Director, Regulatory and Compliance, ABHI
Hear our panel discuss how different countries are navigating the regulatory space within MedTech to ensure regulations don’t prevent innovations which can improve patient outcomes.
‘If we could have a single global framework that would be best.’
Alex Denoon, Partner, and Head of Life Sciences and Regulatory Team, Bristows LLP
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MEET OUR PANEL
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Phil Brown Director, Regulatory and Compliance, ABHI |
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Gabriel Adusei Founder of Triune Technologies Ltd |
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Alex Denoon Partner, and Head of Life Sciences and Regulatory Team, Bristows LLP |
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Mike King Senior Director, Product and Strategy Safety, Regulatory and Quality Technology Solutions |
