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Sinovac Reports Unaudited First Quarter 2012 Financial Results
Date:5/15/2012

al cases, compared to approximately 170,000 reported cases with 62 fatalities in the first four months in 2011.
  • As of May 2012, the dedicated construction and equipment installation for the EV71 production plant in Changping site has been completed.  Currently, the Company is conducting validation of the equipment and production process.  The GMP application for the EV71 plant will be planned according to the clinical development and registration progress.
  • In May 2012, Sinovac completed negotiations with the Shanghai Centers for Disease Control and Prevention (Shanghai CDC) on the details of the Shanghai tender to supply inactivated hepatitis A vaccine in prefilled syringe form.  The total volume of vaccine to be supplied is approximately 420,000 doses, sufficient for one year supply.  Sinovac was selected in December 2011 by the Shanghai CDC as the sole supplier to supply prefilled syringe inactivated hepatitis A vaccine.
  • In March 2012, Sinovac was awarded the government tender to supply Healive to Mongolia.  The total ordered quantity for Mongolia was approximately 191,000 doses, and two deliveries were completed in March and April.
  • According to the GMP inspection plan, the State Food and Drug Administration (SFDA) plans to conduct the official GMP inspection of Sinovac Dalian's mumps vaccine production plant before the end of May 2012.  As previously reported, Sinovac Dalian, an operating subsidiary of the Company, obtained the production license from the SFDA for its mumps vaccine in December 2011, and applied for GMP certification in March 2012.
  • In late April, Sinovac successfully passed the annual follow-up GMP inspection on the Company's influenza vaccine production plant according to Good Manufacturing Practice for Drugs (2010 Revision), or the new GMP guidelines that came into force in 2011.  The inspection was conducted by the SFDA, under the guidance and s
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