Published: August 01, 2011
PPD's Dr. Henrietta Ukwu Honored as Influential Leader for Pioneering Work in Global Regulatory Affairs
WILMINGTON, N.C. - (BUSINESS WIRE) - PPD, Inc. (Nasdaq: PPDI) today announced that Dr. Henrietta Ukwu, senior
vice president for global regulatory affairs, has been named to the 2011 PharmaVOICE
100 list of the most inspiring people in the life sciences industry.
The honor from PharmaVOICE magazine recognizes Dr. Ukwu's
contributions in providing innovative leadership in the area of regulatory
affairs in the endeavor of delivering life-changing medicines for
people in need. An internist and infectious disease physician, Dr. Ukwu
has extensive global regulatory experience across many biopharmaceutical
therapeutic platforms and geographic regions.
"I am honored to be named to the PharmaVOICE 100," Dr. Ukwu said.
"It is humbling to be recognized for the initiatives I've championed and
for my efforts to teach and mentor rising leaders in the life sciences
industry."
Now in its seventh year, the PharmaVOICE 100 is an annual list of
individuals recognized for their contributions to the life sciences
industry. The honorees are nominated by thousands of PharmaVOICE readers.
"The PharmaVOICE 100 are individuals who think outside the box,
pioneer new paths to success and inspire their colleagues in the
industry; they translate industry issues into opportunities and take the
time to mentor the next generation of leaders in the life sciences
arena," said Taren Grom, editor-in-chief and cofounder of PharmaVOICE.
"Dr. Ukwu's demonstrated vision, leadership, and passion for impacting
humanity through the pharmaceutical and CRO industry make her a great
leader and role model."
Dr. Ukwu captured the evolution of the life sciences industry and
regulatory profession, as well as the crucial and strategic role of
regulatory teams in fostering success, in her new book, Global
Regulatory Systems: A Strategic Primer for Biopharmaceutical Product
Development and Registration. The book, published by CenterWatch, is
a comprehensive reference guide for navigating the complexities of
regulatory systems for product development, approval and registration
around the world.
Prior to joining PPD, Dr. Ukwu held senior management positions in
regulatory affairs at Pfizer, Inc., Wyeth Pharmaceuticals, Inc., and
Merck & Co., Inc. She was involved in numerous product development
activities and directly led the successful original regulatory
development and filings of 14 new products, all approved.
About PPD
PPD is a leading global contract
research organization providing drug
discovery, development and lifecycle management services. Our
clients and partners include pharmaceutical, biotechnology, medical
device, academic and government organizations. With offices in 44
countries and more than 11,000 professionals worldwide, PPD applies innovative
technologies, therapeutic
expertise and a commitment to quality to help clients and partners
accelerate the delivery of safe and effective therapeutics and maximize
the returns on their R&D investments. For more information, visit http://www.ppdi.com/.
Except for historical information, all of the statements,
expectations and assumptions, including statements, expectations and
assumptions about Dr. Ukwu's contributions to PPD, contained in this
news release are forward-looking statements that involve a number of
risks and uncertainties. Although PPD attempts to be accurate in making
these forward-looking statements, it is possible that future
circumstances might differ from the assumptions on which such statements
are based and could cause actual results to differ materially from the
forward-looking statements. Other important factors which could cause
future results to differ materially include the following: the ability
to attract, integrate and retain key personnel, including a new CEO;
competition in the outsourcing industry; PPD's ability to win new
business; rapid technological advances that make our services less
competitive; compliance with drug development regulations; changes in
the regulation of the drug development process; overall global economic
conditions; economic conditions in the pharmaceutical, biotechnology and
government-sponsored research sectors; research and development spending
in the pharmaceutical, biotechnology and government-sponsored research
sectors; outsourcing trends in the pharmaceutical, biotechnology and
government-sponsored research sectors; consolidation in pharmaceutical
and biotechnology industries; loss, delay or modification of large
contracts; higher-than-expected cancellation rates; the rate of
conversion of backlog into revenue; actual operating performance;
fluctuations in currency exchange rates; risks associated with and
dependence on strategic relationships; risks associated with fixed price
contracts and cost overruns; international economic and political risks;
and the ability to control SG&A spending. These and other PPD risk
factors are set forth in more detail from time to time in our SEC
filings, copies of which are available free of charge upon request from
PPD's investor relations department. PPD assumes no obligation and
expressly disclaims any duty to update these forward-looking statements
in the future, except as required by applicable law. These
forward-looking statements should not be relied upon as representing
PPD's estimates or views as of any date subsequent to the date hereof.

PPD
Media:
Ned Glascock, 910-558-8760
ned.glascock@ppdi.com
or
Analysts/Investors:
Luke
Heagle, 910-558-7585
luke.heagle@ppdi.com
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