PROLONGATION OF THE FDA APPROVAL PROCEDURE FOR BIOHIT'S GASTROPANEL TESTS


BIOHIT OYJ STOCK EXCHANGE RELEASE ON 7 MAY 2008 AT 09:50 AM                     

PROLONGATION OF THE FDA APPROVAL PROCEDURE FOR BIOHIT'S GASTROPANEL TESTS       

The US Food and Drug Administration (FDA) has demanded further clarifications 
regarding the clearance application for the Pepsinogen I and II tests included  
in the GastroPanel examination. Authorisation was previously expected before the
end of the first half of 2008 but due to the new request the procedure will be  
prolonged. At this stage it is therefore difficult to estimate the schedule for 
the whole approval procedure.                                                   

We will inform about the case later, as we get further information from FDA.    

Osmo Suovaniemi                                                                 
President & CEO                                                                 
Biohit Oyj                                                                      


Further information:                                                            

Osmo Suovaniemi, M.D., Ph.D., Professor                                         
President & CEO                                                                 
Tel: +358-9-773 861                                                             
GSM: +358-40-745 5605                                                           
Email: osmo.suovaniemi@biohit.com                                               

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