Tue, Jan 23
|Zoom
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.
Time & Location
Jan 23, 2024, 5:00 PM EST – Jan 24, 2024, 5:00 PM EST
Zoom
Guests
About the event
Time:
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:
https://unisydney.zoom.us/j/86978141875?from=addon
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,
FDA/ICH GCP, FDA/GMP, USDA, HIPAA, EMEA,
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.