Regulatory Considerations for AI in MedTech

Regulatory Considerations for AI in MedTech

AI in MedTech requires compliance with evolving regulations. Jennifer guides firms on FDA approvals, transparency, and market entry.

By Amplify MedTech

Date and time

Thursday, May 15 · 9 - 10am PDT

Location

Online

Refund Policy

Refunds up to 7 days before event

About this event

  • Event lasts 1 hour

As artificial intelligence continues to revolutionize the medical technology industry, navigating the evolving regulatory landscape is crucial for success. This webinar will provide insights into key regulatory considerations for AI-driven medical devices, including FDA requirements, risk assessment, validation strategies, and emerging global regulatory trends.

Join Jennifer Palinchik and Fehmida Kapadia as they discuss best practices for bringing AI-powered MedTech innovations to market while ensuring safety, efficacy, and compliance. Whether you're a startup, an established MedTech company, or a regulatory professional, this session will equip you with the knowledge to navigate regulatory challenges effectively.

Key Takeaways:

  • The role of regulatory bodies in AI development for medical devices.
  • Key challenges and strategies for achieving compliance.
  • Future trends & evolving regulatory guidance.
  • How to align business strategy with regulatory requirements.
  • Best practices for ensuring patient safety and product efficacy.
  • Insights into the future of AI regulation in the MedTech industry.

Why You Should Attend: This event is a must-attend for anyone involved in the development, approval, or commercialization of AI-powered medical technologies. Don't miss the opportunity to hear from one of the Top Women in MedTech and learn strategies to navigate the rapidly evolving field of AI in healthcare.

Featured Speaker -

Jennifer Palinchik is an accomplished business leader and biomedical engineer with over 20 years of experience in the medical device industry. With extensive product development and market research experience she has led and contributed to more than 130 medical device clearances and has success in growing and sustaining a profitable organization. Her expertise is in providing business strategy consulting to senior executives in large corporations, startups, academic institutions, and healthcare organizations, focusing on strategic business and regulatory decisions. She holds a Bachelor of Science in Biomedical Engineering from the University of Toledo and a Master of Business in Executive Entrepreneurship from Ashland University. Jennifer's contributions have been recognized through prestigious accolades, including Crain's Cleveland Business Top 40 under 40 and multiple honors as one of the Top Women in MedTech. She has also been a guest speaker at the Cleveland Clinic Innovations Summit, Ohio State Senate, and other Medtech conferences.

Moderator -

Dr. Fehmida Kapadia is an expert in entrepreneurship, business strategy, and technology commercialization. As the Founder and President of Kapamed Consulting and Amplify MedTech, she has guided over 100 startups in their journey to success. With a PhD in Biochemistry and a master’s in Biotechnology Entrepreneurship, Dr. Kapadia specializes in strategic partnerships, fundraising, and biomedical product development.

What is the Amplify MedTech Hub?

The Amplify MedTech Hub is building a collaborative MedTech ecosystem in the DMV region. The Hub aims to drive innovation, foster collaboration, and support the development of groundbreaking healthcare solutions. By connecting entrepreneurs, startups, investors, service providers, economic development agencies, and researchers, the Amplify MedTech Hub seeks to revolutionize patient care locally and globally.


Sponsorship Opportunities

Interested in sponsoring the MedTech Hub? We offer several sponsorship packages to help you gain visibility and connect with key players in the DMV MedTech ecosystem.

Contact us to learn more.

amplifymedtech@gmail.com

fehmidak@kapamedinc.com

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