Sinovac's H1N1 Vaccine Passes Experts Evaluation Organized by SFDA

* Reuters is not responsible for the content in this press release.

Mon Aug 31, 2009 8:00am EDT

BEIJING, Aug. 31 /PRNewswire-Asia/ -- Sinovac Biotech Ltd. (NYSE Amex:
SVA), a leading provider of biopharmaceutical products in China, announced
today that Sinovac's H1N1 vaccine has passed the experts evaluation organized
by State Food and Drug Administration (SFDA).  The vaccine is expected to
obtain the production license within this week.
    On August 30 and 31, 2009, State Food and Drug Administration (SFDA)
organized and held an experts evaluation conference focused on A/H1N1 vaccines
to evaluate Sinovac's H1N1 vaccine, which has recently completed a clinical
trial.  Top-line results from the trial demonstrated Sinovac's H1N1 vaccine to
have a good safety profile and immunogenicity factors that reach the EU
criterion after a single shot.  No severe adverse events were reported after
inoculation.  Based on the results of the evaluation, the experts unanimously
agreed that Sinovac's H1N1 vaccine is applicable to all people from 3 to 60
years old and the vaccination schedule is single shot.  The result of the
experts evaluation conference will be submitted to SFDA on September 1st,
which will be the primary opinion for SFDA to issue the production license.
    Sinovac submitted the H1N1 split influenza vaccine without adjuvant for
registration approval, which is applicable to all people from 3 to 60 years
old.  The dosage is 15ug/0.5ml/dose. Only one shot is needed for inoculation.
    Mr. Weidong Yin, Chairman, President and CEO of Sinovac commented, "We are
very excited to see that our H1N1 vaccine has passed the experts evaluation
conference organized by SFDA.  The evaluation result will be the important
opinion for SFDA to issue the production license.  We expect to obtain the
production license within one week.  With this approval, we can continue to
fulfill our mission to provide top-quality vaccines to prevent and control the
spreading of H1N1 virus not only in China, but worldwide."
    About Sinovac
    Sinovac Biotech Ltd. is a China-based biopharmaceutical company that
focuses on the research, development, manufacture and commercialization of
vaccines that protect against human infectious diseases.  Sinovac's vaccine
products include Healive(R) (hepatitis A), Bilive(R) (combined hepatitis A and
B), and Anflu(R) (influenza).  Panflu(TM), Sinovac's pandemic influenza
vaccine (H5N1), has already been approved for government stockpiling.  Sinovac
is developing vaccines for enterovirus 71, universal pandemic influenza,
Japanese encephalitis vaccine, and human rabies vaccine.  Its wholly owned
subsidiary, Tangshan Yian, is conducting field trials for independently
developed inactivated animal rabies vaccines.
    Safe Harbor Statement
    This announcement contains forward-looking statements.  These statements
are made under the "safe harbor" provisions of the U.S. Private Securities
Litigation Reform Act of 1995.  These forward-looking statements can be
identified by words or phrases such as "will," "expects," "anticipates,"
"future," "intends," "plans," "believes," "estimates" and similar statements.
Among other things, the business outlook and quotations from management in
this press release contain forward-looking statements.  Statements that are
not historical facts, including statements about Sinovac's beliefs and
expectations, are forward-looking statements.  Forward-looking statements
involve inherent risks and uncertainties.  A number of important factors could
cause actual results to differ materially from those contained in any forward-
looking statement. Sinovac does not undertake any obligation to update any
forward-looking statement, except as required under applicable law.
    For more information, please contact:

     Helen G. Yang
     Sinovac Biotech Ltd.
     Tel:   +86-10-8289-0088 x9871
     Fax:   +86-10-6296-6910
     Email: info@sinovac.com

    Investors:
     Amy Glynn/Sara Pellegrino
     The Ruth Group
     Tel:   +1-646-536-7023/7002
     Email: aglynn@theruthgroup.com
            spellegrino@theruthgroup.com

    Media:
     Janine McCargo
     The Ruth Group
     Tel:   +1-646-536-7033
     Email: jmccargo@theruthgroup.com

SOURCE  Sinovac Biotech Ltd.

Helen G. Yang of Sinovac Biotech Ltd., +86-10-8289-0088 x9871, Fax
+86-10-6296-6910, info@sinovac.com; or Investors, Amy Glynn & Sara Pellegrino,
+1-646-536-7023/7002, aglynn@theruthgroup.com, spellegrino@theruthgroup.com,
or Media, Janine McCargo, +1-656-536-7033, all of The Ruth Group, for SVA
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