EP 346 - We chat with the founder & CEO of Device Access - who help MedTech companies gain market access and regulatory approval - about how over regulation can stifle innovation and lead to an adverse impact on patient care and outcomes.

Michael Branigan tells us about:

Why US companies aren’t interested infringing their devices to the UK anymore (hint it’s cos we are tiny)

Why regulation is stifling innovation, and how that is bad for all of us, but particularly the NHS

He also mentions Brexit, but not for the reasons that you’d expect.

Chapters:

00:00 BWB with Michael Branagan-Harris

01:51 The Changing Landscape UK MedTech

02:46 Impact of European Medical Device Regulations

04:46 Challenges in the MedTech Industry

05:55 Gov Initiatives and Their Shortcomings

07:28 Understanding Medical Device Regulations

14:42 The Role of NICE and Market Access

28:56 The Future of MedTech and Market Strategies

35:22 Affordability vs. Innovation in Healthcare

37:00 Challenges in Medtech vs. Pharma

37:39 Navigating the NHS Procurement Process

38:59 Leveraging Data for Healthcare Solutions

41:53 Global Perspectives on Healthcare Systems

49:20 The Role of MedTech in Modern Healthcare

52:12 Independent Clinical Evidence

55:34 Quick Fire Round - Get to Know Michael

01:00:06 Wrap Up and Advice for Entrepreneurs

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