AI and Medical Product Development

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.