BioSyent Inc. ("BioSyent") (TSX VENTURE:RX) today released a summary of its 2010
second quarter (Q2) financial results. 


Total Sales were 62% higher at $599,055 in the first half of 2010 compared to
$370,673 in the first half of 2009. The sales in Q2 2010 were 9% higher at
$288,099 compared to $263,622 in Q2 2009. 


Gross Margins increased from 58.5% in the first half of 2009, to 70.5% in the
first half of 2010 primarily because of lower sales of lower margin products and
proportionately higher sales of FeraMAX(R) and Protect-It(R).


The Company incurred a loss of ($159,376) in the first half of 2010, 31% lower
than a loss of ($232,108) in the first half of 2009. 


Full details of 2010 second quarter results including June 30, 2010 Financial
Statements and Management's Discussion & Analysis will be posted on sedar.com on
August 17, 2010.


BioSyent Inc. continues to concentrate on its pharmaceutical strategy to source
products that have been successfully developed and proven to be safe and
effective; manage these products through the regulatory process and product
registration (approval); and once approved, market these products in Canada.
These pharmaceuticals will compete in both the branded and generic market
segments and will not require further product development investment other than
regulatory costs. 


BioSyent Inc. is a publicly traded specialty pharmaceutical company whose wholly
owned subsidiary, BioSyent Pharma Inc., sources, acquires or in-licences
pharmaceutical products and markets these products in Canada. Wholly owned
BioSyent subsidiary Hedley Technologies Ltd. operates the company's legacy
business marketing bio and health friendly non-chemical insecticides. BioSyent
common shares are listed for trading on the TSX Venture Exchange (TSXV) under
the symbol RX.


This press release may contain information or statements that are
forward-looking.  The contents herein represent our judgment, as at the release
date, and are subject to risks and uncertainties that may cause actual results
or outcomes to be materially different from the forward-looking information or
statements.  Potential risks may include, but are not limited to, those
associated with clinical trials, product development, future revenue,
operations, profitability and obtaining regulatory approvals.


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