Experts from PAREXEL Consulting will present insights into achieving regulatory approval at the BIO International Convention, May 18 -21, 2009 at the Georgia World Congress Center in Atlanta, Georgina.
On Tuesday, May 19 of the convention, PAREXEL Consulting experts will present on the following panels, which are part of the Achieving Regulatory Approval Breakout Session:
Regulatory Best Practices for Emerging Companies and First-Time Filers
Panelist: David Morse, Principal Consultant, PAREXEL Consulting
(8:00 a.m. – 9:30 a.m.)
Is Gaining Drug Approval More Difficult in Europe than the U.S., or Vise Versa?
Panelist: Alberto Grignolo, Ph.D., Corporate Vice President, PAREXEL Consulting
(4:00 p.m. – 5:30 p.m.)
If you would like to meet with us at BIO 2009 in Atlanta, please attend one of the above sessions or contact Elizabeth Thomae at
+1 303-284-4074, or elizabeth.thomae@parexel.com
PAREXEL has worked with the top 10 global biotechnology companies, and has helped hundreds of small and mid-size biopharmaceutical companies develop and implement biologics product and regulatory strategies aimed at maximizing product value at every milestone and phase of development, around the world.
Our key expertise areas include:
Downloadable information: