Utah RAPS Chapter St. George Event at Utah Tech
What does it actually take to get a software-based medical device into the hands of clinicians? Software devices, digital health products, wearables, and AI all have the possibility of revolutionizing the health landscape. With great engineering, great regulatory strategy, great clinical results, and great commercial potential, you have a real shot. Chris Phillips will speak about his real-world experience bringing novel software technologies to market in the USA. We’ll address some common hurdles of the regulatory process, and how you can use regulatory strategy to build a winning product strategy for your new advanced technologies.
Utah Tech University
225 S Univ Ave
St. George, UT 84770
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation. All cancellation requests must be submitted in writing to [email protected]. Cancellations will receive a full refund minus a 20% administrative fee. RAPS is unable to accept cancellations by phone.
Paid registration substitutions may be accepted with written approval from RAPS for requests received before the start of the event. To transfer a registration, email [email protected] with the event title, name of the original registrant and the contact information for the new attendee.
A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.
Contact the RAPS Support Center:
Call +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email [email protected].


VP, Regulatory Affairs & Quality, Epitel
Chris Phillips is a leader in Medical Device and MedTech strategy and organization, with over 20 years of experience in Regulatory Affairs, Quality Systems, and Clinical Affairs covering a wide range of devices. Chris has helped bring innovative medical devices to market in the USA, Europe, Canada, Australia, Brazil and other global markets; and has built and maintained ISO 13485- and 21 CFR 820-compliant Quality Management Systems. Chris has played key roles in designing, developing, and launching novel software- and AI-based medical devices, digital health software products, implantable medical devices, and disposable medical devices. He has also helped develop preclinical and clinical studies, including clinical trials of novel devices and clinical evaluations of established products. Chris possesses extensive knowledge and understanding of requirements of the FDA, European Medical Device Regulation, Canadian Medical Devices Regulation, and other international regulations. Chris has an MSHS with a focus in Regulatory Affairs and holds RAC and CMDA certifications.We have completed our migration to a new platform and are pleased to introduce the updated site.
What to expect: If you have an existing login, please RESET YOUR PASSWORD before signing in. After you log in for the first time, you will be prompted to confirm your profile preferences, which will be used to personalize content.
We encourage you to explore the new website and visit your updated My RAPS page. If you need assistance, please review our FAQ page.
We welcome your feedback. Please let us know how we can continue to improve your experience.