Regulatory strategy for founders and policy makers episode artwork

EPISODE · Apr 22, 2025 · 55 MIN

Regulatory strategy for founders and policy makers

from Global Perspectives on Digital Health · host Shubs Upadhyay

Practical breadth and depth on the global state of regulation from someone at the cutting edge of regulatory policy. Shubs welcomes Hugh Harvey, founder of Hardian Health and a regulatory expert in digital health. Shubs and Hugh discuss the complex landscape of medical device regulation worldwide, with emphasis on how these frameworks impact digital health innovation in low and middle-income countries (LMICs). Guest BackgroundHugh Harvey is a former radiologist who transitioned to the digital health industry. After working at Babylon Health and serving as Clinical Director at Kheiron Medical (where they secured Europe's first CE mark for a deep learning-based breast cancer detection device), Hugh founded Hardian Health to help companies navigate regulatory pathways for AI and digital health solutions.Key Discussion PointsThe Global State of Medical Device RegulationRegulatory Variation: Hugh explains the significant differences in regulatory approaches between regions like the EU (stricter) and the US (increasingly deregulatory)(Some) LMIC Contexts: Only about 40% of African countries have actual medical device regulations, with only South Africa having comprehensive frameworksCybersecurity Risks: Medical health data sells for more than financial data on black markets, making robust regulation essential for protecting patientsChallenges for Digital Health InnovatorsFounder Misconceptions: Many startups allocate insufficient resources for regulatory compliance. Regulatory compliance should represent 5-10% of a company's overall budget.Regulatory Debt: Postponing regulatory considerations creates compounding challenges that become increasingly difficult to address later down the lineLarge Language Models: Hugh's skepticism about LLMs in healthcare, noting they're "massively overrated" for medical reasoning tasks and face significant regulatory hurdles, and yet Hugh sees some promise over the hill. Practical Guidance for Digital Health CompaniesGetting the mindset right: Thinking about it in the same way you might approach a driving test. Universal Standards: Quality management systems (ISO 13485) are increasingly harmonized globallyApproach in LMICs: Thinking about deploying in an place where there is little to no regulatory structure? You might want to consider securing certification in countries with established regulatory pathways prior, and then work with the local government.What Regulators Could Do BetterProactivity: Regulators should be more proactive in providing guidance on novel technologiesTransparency: More open sharing of regulatory decisions would help the entire industry move forwardCapacity: Governments should increase funding for regulatory bodies to reduce backlogs and improve efficiencyChapters00:00 Introduction and Background04:22 The State of Regulation in Healthcare06:36 Why so regulated?09:24 Global Perspectives on Regulatory Approaches16:53 Harmonization of Global Standards19:34 Recommendations for Regulators31:53 Regulatory strategy for founders: The Driving Analogy42:14 What if there is little or no regulatory enforcement where I operate?43:59 The Five Stages of Regulatory Grief47:44 Hugh's spicy takes 🌶️Key Quotes"Regulations are written in blood... the reason regulations/FDA are as they are today is because of events like thalidomide."What's the cost of not being compliant? Well, it's everything, it's your entire business model.""The attack surface vector, especially under these generative AI models, is huge, vast, and frankly, completely unknown."Hugh provides a compelling case for embracing regulatory requirements as not just necessary obligations but strategic advantages. While acknowledging the challenges of navigating complex regulatory landscapes, particularly for innovators working in regions with limited frameworks, he offers practical guidance on approaching compliance as a foundation for long-term success in digital health. You can find Hugh and his work at hardianhealth.comLiked this episode? You might also like these:Episode 3: Bilal MateenEpisode 5: Prof Stephen Gilbert 💕 If you found this podcast episode helpful, please leave a comment, give us a 5 star review and share with your colleagues and people who would find this useful. It helps us reach the people who are implementing and could find this useful in creating an impact with digital health in LMICs. Check out the Substack here

Practical breadth and depth on the global state of regulation from someone at the cutting edge of regulatory policy. Shubs welcomes Hugh Harvey, founder of Hardian Health and a regulatory expert in digital health. Shubs and Hugh discuss the complex landscape of medical device regulation worldwide, with emphasis on how these frameworks impact digital health innovation in low and middle-income countries (LMICs). Guest BackgroundHugh Harvey is a former radiologist who transitioned to the digital health industry. After working at Babylon Health and serving as Clinical Director at Kheiron Medical (where they secured Europe's first CE mark for a deep learning-based breast cancer detection device), Hugh founded Hardian Health to help companies navigate regulatory pathways for AI and digital health solutions.Key Discussion PointsThe Global State of Medical Device RegulationRegulatory Variation: Hugh explains the significant differences in regulatory approaches between regions like the EU (stricter) and the US (increasingly deregulatory)(Some) LMIC Contexts: Only about 40% of African countries have actual medical device regulations, with only South Africa having comprehensive frameworksCybersecurity Risks: Medical health data sells for more than financial data on black markets, making robust regulation essential for protecting patientsChallenges for Digital Health InnovatorsFounder Misconceptions: Many startups allocate insufficient resources for regulatory compliance. Regulatory compliance should represent 5-10% of a company's overall budget.Regulatory Debt: Postponing regulatory considerations creates compounding challenges that become increasingly difficult to address later down the lineLarge Language Models: Hugh's skepticism about LLMs in healthcare, noting they're "massively overrated" for medical reasoning tasks and face significant regulatory hurdles, and yet Hugh sees some promise over the hill. Practical Guidance for Digital Health CompaniesGetting the mindset right: Thinking about it in the same way you might approach a driving test. Universal Standards: Quality management systems (ISO 13485) are increasingly harmonized globallyApproach in LMICs: Thinking about deploying in an place where there is little to no regulatory structure? You might want to consider securing certification in countries with established regulatory pathways prior, and then work with the local government.What Regulators Could Do BetterProactivity: Regulators should be more proactive in providing guidance on novel technologiesTransparency: More open sharing of regulatory decisions would help the entire industry move forwardCapacity: Governments should increase funding for regulatory bodies to reduce backlogs and improve efficiencyChapters00:00 Introduction and Background04:22 The State of Regulation in Healthcare06:36 Why so regulated?09:24 Global Perspectives on Regulatory Approaches16:53 Harmonization of Global Standards19:34 Recommendations for Regulators31:53 Regulatory strategy for founders: The Driving Analogy42:14 What if there is little or no regulatory enforcement where I operate?43:59 The Five Stages of Regulatory Grief47:44 Hugh's spicy takes 🌶️Key Quotes"Regulations are written in blood... the reason regulations/FDA are as they are today is because of events like thalidomide."What's the cost of not being compliant? Well, it's everything, it's your entire business model.""The attack surface vector, especially under these generative AI models, is huge, vast, and frankly, completely unknown."Hugh provides a compelling case for embracing regulatory requirements as not just necessary obligations but strategic advantages. While acknowledging the challenges of navigating complex regulatory landscapes, particularly for innovators working in regions with limited frameworks, he offers practical guidance on approaching compliance as a foundation for long-term success in digital health. You can find Hugh and his work at hardianhealth.comLiked this episode? You might also like these:Episode 3: Bilal MateenEpisode 5: Prof Stephen Gilbert 💕 If you found this podcast episode helpful, please leave a comment, give us a 5 star review and share with your colleagues and people who would find this useful. It helps us reach the people who are implementing and could find this useful in creating an impact with digital health in LMICs. Check out the Substack here

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Regulatory strategy for founders and policy makers

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Frequently Asked Questions

How long is this episode of Global Perspectives on Digital Health?

This episode is 55 minutes long.

When was this Global Perspectives on Digital Health episode published?

This episode was published on April 22, 2025.

What is this episode about?

Practical breadth and depth on the global state of regulation from someone at the cutting edge of regulatory policy. Shubs welcomes Hugh Harvey, founder of Hardian Health and a regulatory expert in digital health. Shubs and Hugh discuss the complex...

Is there a transcript available for this episode?

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