DRAXIS Appoints Bruce DeChambre to Head Business Development for Contract Manufacturing Division
May 29 2007 - 9:00AM
PR Newswire (US)
MISSISSAUGA, ON, May 29 /PRNewswire-FirstCall/ -- DRAXIS Pharma,
the contract manufacturing division of DRAXIS Health Inc. (TSX:
DAX) (NASDAQ: DRAX), has appointed Bruce DeChambre as Vice
President Commercial and Business Development. Mr. DeChambre is
charged with identifying prospective customers and developing new
business opportunities within the blue chip pharmaceutical sector
while continuing to deliver superior service to DRAXIS Pharma's
client base. He has over 25 years of progressive pharmaceutical
sales, marketing and business development experience with US-based
and international companies, including senior management
responsibilities in the contract manufacturing sector. Prior to
joining DRAXIS Pharma, Mr. DeChambre was a pharmaceutical industry
consultant to investment firms and healthcare advertising agencies.
Previously, he was Vice President Sales and Marketing at
SAB-Pharma, the U.S. marketing arm of Sabex Inc., which was
recently acquired by Novartis. He also served as Vice President
Business Development for Cardinal Health's Sterile Technology
Group, a contract manufacturer of sterile pharmaceuticals. In
addition, Mr. DeChambre has served in senior sales and marketing
management positions at Abraxis Pharmaceutical (formerly American
Pharmaceutical Partners, Inc.), Fujisawa USA, Inc. and Baxter
Healthcare Corporation. Mr. John Durham, President of DRAXIS
Pharma, stated, "We are pleased and excited to have Bruce join our
management team. He brings a wealth of business development
experience plus a broad network of senior level contacts in the
pharmaceutical and biotechnology industries. His expertise in the
sterile products area of the contract manufacturing sector is
particularly relevant, given DRAXIS Pharma's strength and focus in
the production of sterile injectables, ointments and creams as well
as our expanding capabilities in sterile lyophilization." "DRAXIS
Pharma offers a full range of contract manufacturing capabilities
and is an organization committed to quality, absolute customer
satisfaction and excellence in regulatory compliance, with a
facility that has a solid tradition of pharmaceutical
manufacturing," noted Mr. DeChambre. "My immediate priorities are
to enhance the effectiveness of our commercial organization,
increase awareness in the pharmaceutical industry about the
outstanding capabilities and personnel we have at DRAXIS Pharma,
and build momentum by attracting new business." DRAXIS Pharma, a
division of DRAXIS Specialty Pharmaceuticals Inc., operates a
cGMP-compliant 247,000 square foot facility located in Kirkland,
Quebec just outside Montreal and has production capabilities for a
broad range of pharmaceutical dosage forms; injectable, oral and
topical including sterile and non-sterile products. In 2005 DRAXIS
Pharma expanded its capacity to produce sterile lyophilized
(freeze-dried) injectable products in vials and in 2006 further
expanded its capacity to produce sterile injectable liquids in
vials and ampoules. About DRAXIS Health Inc. DRAXIS Health, through
its wholly owned operating subsidiary, DRAXIS Specialty
Pharmaceuticals Inc., provides products in three categories:
sterile products, non-sterile products and radiopharmaceuticals.
Sterile products include liquid and freeze-dried (lyophilized)
injectables plus sterile ointments and creams. Non-sterile products
are produced as solid oral and semi-solid dosage forms.
Radiopharmaceuticals are used for both therapeutic and diagnostic
molecular imaging applications. Pharmaceutical contract
manufacturing services are provided through the DRAXIS Pharma
division and radiopharmaceuticals are developed, produced, and sold
through the DRAXIMAGE division. DRAXIS employs approximately 500
staff in its Montreal facility. For additional information please
visit http://www.draxis.com/. Caution Concerning Forward-Looking
Statements This news release contains forward-looking statements
within the meaning of Section 27A of the Securities Act of 1933, as
amended (the "Securities Act") and Section 21E of the Securities
Exchange Act of 1934, as amended (the "Exchange Act") and as
contemplated under other applicable securities legislation. These
statements can be identified by the use of forward-looking
terminology such as "may," "will," "expect," "anticipate,"
"estimate," "continue," "plan," "intend," "believe" or other
similar words. These statements discuss future expectations
concerning results of operations or financial condition or provide
other forward-looking information. Our actual results, performance
or achievements could be significantly different from the results
expressed in, or implied by, those forward-looking statements. You
should not place undue reliance on any forward-looking statement,
which speaks only as of the date made. These statements are not
guarantees of future performance. By their nature, forward-looking
statements involve numerous assumptions, known and unknown risks,
uncertainties and other factors that may cause the actual results
or performance of the Company to be materially different from such
statements or from any future results or performance implied
thereby. Factors that could cause the Company's results or
performance to differ materially from a conclusion, forecast or
projection in the forward-looking statements include, but are not
limited to: - the achievement of desired clinical trial results
related to the Company's pipeline products; - timely regulatory
approval of the Company's products; - the ability to comply with
regulatory requirements applicable to the manufacture and marketing
of the Company's products; - the Company's ability to obtain and
enforce effective patents; - the non-infringement of third party
patents or proprietary rights by the Company and its products; -
factors beyond our control that could cause interruptions in our
operations in our single manufacturing facility (including, without
limitation, material equipment breakdowns); - reimbursement
policies related to health care; - the establishment and
maintenance of strategic collaborative and commercial
relationships; - the Company's dependence on a small number of key
customers; - the disclosure of confidential information by our
collaborators, employees or consultants; - the preservation of
healthy working relationships with the Company's union and
employees; - the Company's ability to grow the business; - the
fluctuation of our financial results and exchange and interest rate
fluctuations; - the adaptation to changing technologies; - the loss
of key personnel; - the avoidance of product liability claims; -
the loss incurred if current lawsuits against us succeed; - the
volatility of the price of our common shares; - market acceptance
of the Company's products; and - the risks described in "Item 3.
Key Information - Risk Factors" in the Annual Report Form 20-F
filed by the Company with the United States Securities and Exchange
Commission and which is also filed as the Company's Annual
Information Form with Canadian securities regulators. For
additional information with respect to certain of these and other
factors, and relating to the Company generally, reference is made
to the Company's most recent filings with the United States
Securities and Exchange Commission (available on EDGAR at
http://www.sec.gov/) and the filings made by the Company with
Canadian securities regulators (available on SEDAR at
http://www.sedar.com/). The forward-looking statements contained in
this new release represent the Company's expectations as at May 28,
2007. Unless otherwise required by applicable securities laws, the
Company disclaims any intention or obligation to update or revise
any forward-looking statements, whether as a result of new
information, future events or otherwise. DATASOURCE: DRAXIS Health
Inc. CONTACT: DRAXIS Health Inc., Jerry Ormiston, Executive
Director, Investor Relations, Tel: (877) 441-1984
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