Episode description

In this episode, host Etienne Nichols speaks with Christine Luk, Associate Regulatory Affairs Manager at Proxima, about her journey through the medical device sector. From her academic beginnings in biochemistry and biomedical engineering to founding a startup and navigating FDA regulatory pathways, Christine offers a wealth of knowledge. The discussion delves into the intricacies of working with regulatory consultants, the significance of FDA interactions, and practical tips for medical device startups aiming to maneuver through regulatory challenges successfully.

• [00:02:30] Christine's journey from biochemistry to medical device innovation
• [00:15:00] Insights on starting a medtech startup and the early failures
• [00:30:45] Effective collaboration with regulatory consultants
• [00:45:10] Handling FDA interactions and strategic submissions
• [01:00:20] Advice for medtech startups on navigating regulatory environments

• "You're pitching all these awesome capabilities of your device, meanwhile on the FDA side, we're asking, who are you most like?" – Christine Luk
• "Every meeting is money. Making sure everybody is aligned and on the same page is crucial when dealing with consultants." – Christine Luk

• Engage with local medtech communities and resources, such as accelerators or innovation hubs.
• Early interactions with the FDA can significantly influence your device’s regulatory pathway.
• Thorough documentation and clear communication with consultants are essential for effective project management.

• Texas Medical Center Innovation Institute
• Proxima Clinical Research
• Christine Luk on LinkedIn
• Etienne Nichols on LinkedIn

Feedback is crucial! Please email us your thoughts on this episode and suggestions for future topics at podcast@greenlight.guru

Don’t forget to leave us a review on iTunes!

This episode is proudly sponsored by Greenlight Guru, a global leader in MedTech-specific software solutions. Whether you're in the clinical trial phase or ensuring compliance with quality standards, Greenlight Guru offers tailored solutions to streamline your processes. Their software is designed specifically for the medical device industry, helping companies accelerate their product development with confidence and compliance. Learn more about how Greenlight Guru can illuminate your path to market success by visiting their website at Greenlight Guru. Equip your team with the tools to simplify quality management and keep your focus on innovation and patient safety.