top of page

Tue, Jan 23



AI and Medical Product Development

Learn about the rapidly changing environment with AI, types of AI applications, existing barriers, potential enablers, and projected future of AI in the development of medical devices, while evaluating US and European regulatory policies evolving.

Registration is closed
See other events
AI and Medical Product Development
AI and Medical Product Development

Time & Location

Jan 23, 2024, 5:00 PM EST – Jan 24, 2024, 5:00 PM EST



About the event


Jan 23rd, 5 pm, Eastern time, USA

Jan 24th, 2 am, Middle East

Jan 24th, 9 am, Sydney, Australia

Jan 24th, 6 am, Hong Kong

Zoom Link:

Diane Earp, currently serves as the Vice

President of Regulatory Compliance at the

Research Triangle Institute (RTI), providing

leadership on corporate initiatives regarding

regulatory affairs, quality assurance, security

clearance, compliance, and documentation

management. She is the institutional liaison on

regulatory and quality matters involving

regulatory strategies for FDA/EPA/OECD GLP,


OLAW, OSHA, and other research regulations

and provides expertise to project teams

throughout RTI International. She has over 20

years of experience working effectively with

regulatory agencies and governing bodies and

currently oversees regulatory affairs and quality

assurance personnel and activities for a variety

of programs and contract operations across

four international business units with more

than 6000 personnel throughout the world.

Share this event

bottom of page