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ORGANIZER:MAILTO:webcentral@uc.edu
DTSTART:20251112T170000Z
DTEND:20251112T180000Z
LOCATION: Medical Sciences Building (MSB) Room E255 and via Microsoft Teams
UID:20260622T035336Z@uc.edu
DTSTAMP:20260622T035336Z
SUMMARY:COM Faculty Development: Medpace Series:   How Regulatory Agencies and Regulations Shape Drug Development
DESCRIPTION:<p style="margin-left:0px; margin-right:0px">Medpace and UC have partnered to bring &quot;<em><strong>Charting the Course of Drug Development</strong></em>&quot; seminar series to campus (in-person &amp; virtual) as part of the Research Development workshop offerings. The second seminar in the series will highlight:</p>

<ul>
	<li>Roles and responsibilities in drug development, including IRBs, IBCs, ECs, and RAs</li>
	<li>Regulatory pathways for drug development</li>
	<li>Interface with pharmaceutical industry and investigators</li>
</ul>

<p style="margin-left:0px; margin-right:0px"><strong>Medpace Speakers:&nbsp;&nbsp;<em>Scott Proestel, MD, Vice-President, Medical Dept and Joe Facciolo, MBA, Sr. Manager, Regulatory Affairs</em></strong></p>

<p style="margin-left:0px; margin-right:0px"><strong><em>In-person attendance preferred</em></strong></p>

PRIORITY:5
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