[vc_row][vc_column][vc_message]Check back regularly for additional information on Pre-Conference tracks[/vc_message][vc_column_text]
Wednesday May 27, 2020
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GRP Workshop
Confirmed regulators include: FDA, EMA, PEI, PMDA and Swissmedic.
The highly interactive program will feature presentations and case studies on sterility controls, post manufacturing processing, combination products, and considerations following rapid approvals.[/vc_column_text][/vc_column][vc_column width=”1/4″][vc_column_text]
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Organizing Committee
[/vc_column_text][vc_empty_space height=”10px”][/vc_column][/vc_row][vc_row][vc_column width=”1/2″][vc_column_text]Karen Nichols, Esq.
Co-Chair
Magenta Therapeutics
United States
Yong Fan, MD
A2Z Reg Solutions
United States
Christopher Bravery, PhD
Consulting on Advanced Biologicals
United Kingdom
Scott Burger, MD
Advanced Cell & Gene Therapy
United States[/vc_column_text][/vc_column][vc_column width=”1/2″][vc_column_text]Dominic Wall, PhD, FFSc(RCPA)
Co-Chair
Cell Therapies Pty Ltd, Peter MacCallum Cancer Centre
Australia
Srinivasan Kellathur, PhD
Advanced Therapy Products Unit, Health Sciences Authority
Singapore
Janet Macpherson, PhD
GE Life Sciences
Australia[/vc_column_text][/vc_column][/vc_row][vc_row][vc_column][vc_empty_space height=”10px”][vc_empty_space height=”10px”]
MSC Track

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