PPD, Inc. (Nasdaq: PPDI) today announced it has appointed Edward Ian as
vice president of clinical development for Asia Pacific. Mr. Ian will be
based in Singapore and will provide strategic leadership and operational
oversight for PPD’s Phase II-IV business in the region.
“Edward Ian brings more than 15 years of clinical operations, central
laboratory management, quality management systems and project management
expertise through his long tenure with multinational companies in Asia
Pacific and the United States,” said Paul Colvin, executive vice
president of global clinical development at PPD. “His expertise across a
wide range of areas within the clinical research industry will play a
significant role in advancing our strong position in this growing
region.”
Mr. Ian spent six years at a large, global contract research
organization where he most recently served as executive director of
scientific affairs responsible for Phase I-IV clinical operations in
Asia Pacific. He also held the positions of regional director of
operations and senior director of clinical operations for Asia Pacific,
where he managed daily operations, set strategy and performance
standards, and collaborated on business development initiatives. He
began his career as a laboratory scientist and later served as director
of business development and quality assurance for a regional CRO in
Taiwan where he rose to executive vice president.
Mr. Ian earned his executive master’s of business administration from
National Chengchi University in Taipei, Taiwan, and his bachelor of
science in medical technology from Central Missouri State University in
Warrensburg, Mo.
PPD is one of the largest CROs operating in Asia Pacific with nearly
1,400 people and offices in 13 countries. The company offers a full
range of drug discovery and development services from the region,
including operating global central laboratories in China and Singapore.
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 www.ppdi.com.
Except for historical information, all of the statements,
expectations and assumptions, including statements, expectations and
assumptions about the above named employee's performance and
contributions to PPD and its clinical development business in Asia
Pacific, 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;
international economic and political risks; overall global economic
conditions; economic conditions and outsourcing trends in the
pharmaceutical, biotechnology and government-sponsored research sectors;
consolidation in pharmaceutical and biotechnology industries; PPD’s
ability to win new business; 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
acquisitions and investments, such as impairments and integration rapid
technological advances that make our services less competitive; risks
associated with fixed price contracts and cost overruns; compliance with
drug development regulations; changes in the regulation of the drug
development process; risks that we may increase, reduce or discontinue
our annual dividend policy; 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.

Source(s) : PPD, Inc.