AUG 2019 - Invited Speaker: FDA Translational Medical Device Development Process: An Executive Overview
McGowan Institute for Regenerative Medicine - University of Pittsburgh
JAN 2019 - Invited Speaker: Regulatory Practicum Preclinical Development to Enable Clinical Studies: What Does FDA Require?
Michigan-Pittsburgh-Wyss Regenerative Medicine Resource Center 2nd Semi-Annual Meeting
MAY 2018 - Invited Panelist: Building Product Value: Clinical, Regulatory and Reimbursement Strategies Critical to Impact Commercial Success
Michigan Growth Capital Symposium (MGCS) - Hosted by BioArbor/MichBio
NOV 2017 - FDA Regulatory Sciences for Evaluating Dental Products - Guest Lecture - Research Methods in Periodontics 610 Course, University of Michigan School of Dentistry
OCT 2017 - FDA Engineering Design Control Process Overview - Guest Lecture
Biomedical Design-BME451 Course-College of Engineering, University of Michigan
FEB 2016 - Regulatory Strategy Development Workshop
Graduate Innovative Design In Biomedical Engineering-BME599 Course-College of Engineering, University of Michigan
MAY 2015 - GLP & The GxP Continuum: 'An Overview For Research Principal Investigators & Their Laboratory Teams' - Webinar
For further details regarding upcoming presentations, please contact us at email@example.com
Frequently Requested Talks:
» FDA MEDICAL PRODUCT APPROVALS:
'The Translational Development Process: From Bench-To-Bedside & Beyond'
'Good Clinical Practice & Tips for Great Clinical Research Outcomes'
(AKA: "Clinical Research is Like Football")
» FDA BIMO INSPECTIONS:
'Preparing For BIMO Inspections: What Should Your Clinical Team Expect?'
» FDA IND/IDE:
'The FDA IND/IDE Regulatory Submission Process Overview
Please contact us to schedule a dynamic speaker for your next conference, seminar, meeting or special event by sending us an e-mail request at: firstname.lastname@example.org