Regulatory strategy for founders and policy makers

Описание: 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 Background
Hugh 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 Points

The Global State of Medical Device Regulation
Regulatory 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 frameworks
Cybersecurity Risks: Medical health data sells for more than financial data on black markets, making robust regulation essential for protecting patients

Challenges for Digital Health Innovators
Founder 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 line
Large 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 Companies
Getting 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 globally
Approach 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 Better
Proactivity: Regulators should be more proactive in providing guidance on novel technologies
Transparency: More open sharing of regulatory decisions would help the entire industry move forward
Capacity: Governments should increase funding for regulatory bodies to reduce backlogs and improve efficiency

Chapters

00:00 Introduction and Background
04:22 The State of Regulation in Healthcare
06:36 Why so regulated?
09:24 Global Perspectives on Regulatory Approaches
16:53 Harmonization of Global Standards
19:34 Recommendations for Regulators
31:53 Regulatory strategy for founders: The Driving Analogy
42:14 What if there is little or no regulatory enforcement where I operate?
43:59 The Five Stages of Regulatory Grief
47:44 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.com

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