PharmaNet Development Group to Present at the FBR Capital Markets 12th Annual Spring Investor Conference on Thursday May 29, 2008
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PharmaNet Development Group, Inc. (NASDAQ: PDGI) today announced that
Jeffrey P. McMullen, president and chief executive officer, will make a
presentation on the Company at the FBR Capital Markets 12th
Annual Spring Investor Conference on Thursday May 29, 2008 at 9:00 am
EDT. The conference will take place at the Grand Hyatt New York.
A live audio webcast of the presentation will be accessible directly
from http://www.wsw.com/webcast/fbr21/pdgi/
or from the investor tab of the Company web site at www.pharmanet.com.
The replay of the webcast will be available on the day of the
presentation for approximately ninety days on the Company web site.
About PharmaNet Development Group,
Inc.
PharmaNet Development Group, Inc., a global drug development services
company, provides a comprehensive range of services to the
pharmaceutical, biotechnology, generic drug and medical device
industries. The Company offers clinical-development solutions including
early and late stage consulting services, Phase I clinical studies and
bioanalytical analyses, and Phase II, III and IV clinical development
programs. With approximately 2,600 employees and more than 42 facilities
throughout the world, PharmaNet is a recognized leader in outsourced
clinical development. For more information, please visit our website at www.pharmanet.com.
Forward-Looking Statements
Certain statements made in this press release are forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995 (the "Act"). Additionally, words such as "seek,"
"intend," "believe," "plan," "estimate," "expect," "anticipate" and
other similar expressions are forward-looking statements within the
meaning of the Act. Some or all of the results anticipated by these
forward-looking statements may not occur. Factors that could cause or
contribute to such differences include, but are not limited to, industry
trends and information; whether the Company will achieve its estimated
value relating to discontinued operations; developments with respect to
the SEC's inquiry and securities class action lawsuits and derivative
lawsuits; the Company’s ability to
successfully achieve and manage the technical requirements of
specialized clinical trial services, while complying with applicable
rules and regulations; regulatory changes; changes affecting the
clinical research industry; a reduction of outsourcing by pharmaceutical
and biotechnology companies; the Company’s
ability to compete internationally in attracting clients in order to
develop additional business; the Company’s
evaluation of its backlog and the potential cancellation of contracts;
its ability to retain and recruit new employees; its clients' ability to
provide the drugs and medical devices used in its clinical trials; the
Company’s future stock price; the Company’s
assessment of its current or future effective tax rate; the Company’s
assessment of the value of its deferred tax assets; the Company’s
financial guidance; the Company’s anticipated
capital expenditures; the Company’s ability
to remediate its material weaknesses; the Company’s
costs associated with compliance of Section 404 of the Sarbanes-Oxley
Act; the impact on the Company of foreign currency transaction costs and
the effectiveness of any hedging strategies it implements; the potential
liability associated with the Company’s
registration of its employees’ stock purchase
plan; and the national and international economic climate as it affects
drug development operations.
Further information can be found in the Company’s
risk factors contained in its Annual Report on Form 10-K for the year
ended December 31, 2007 and its most recent Quarterly Report on Form
10-Q. The Company does not undertake to update the disclosures made
herein, and you are urged to read our filings with the Securities and
Exchange Commission.