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GENERAL MANAGER, MANUFACTURING GROUP
TODD BAKER, 973-920-7118
The Building Blocks of
Looking back to look forward.
Breaking Bad: When It Comes
to Technology Transfer,
Old Habits Die Hard
You know you should be using the FDA
2011 Process Validation (PV) Guidance,
so why aren’t you?
EDITORIAL ADVISORY BOARD
Michael J. Beier,
Senior Vice President of Operations
TITAN PHARMACEUTICALS, INC.
Dr. James V. Blackwell, PhD, Consultant
BIOPROCESS TECHNOLOGY CONSULTANTS, INC.
Ronald C. Branning,
Vice President Global Quality
Robert F. Dream, Vice President
H.D.R. COMPANY LTD.
18 Finding Your Niche as a CDMO
Johanna Carmel Egan,
VGP Project Management
CDMO Tapemark possesses not
only a broad range of capabilities in
transdermal patches and oral thin films,
but also a Midwestern commitment to
Girish Malhotra, President
Allan F. Pfitzenmaier, President
VECTECH PHARMA CONSULTANTS INC.
Susan Polizzotto, Manager,
R&D QA GMP Compliance
US SANOFI PASTEUR
Carlos Villalobos, Sr. Dir. Global Engineering
Despite how far we have come, there is
still ample room to grow.
Richard G. Whitfield, Senior Director
Patrick Wong, Director of Global Engineering
BRISTOL-MYERS SQUIBB (BMS)
Validating Disinfection Protocols
for Regulatory Compliance &
It is a regulatory requirement that
the disinfection procedures used in
cleanrooms have to be shown to be
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6, 7, 13 What’s Hot in Innovation
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30 What’s Trending on PharmPro.com
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